Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine

Bayer162 enrolled

Overview

The objectives of the study are to evaluate the analgesic and hypnotic efficacy of naproxen sodium and diphenhydramine combination when compared to naproxen sodium, diphenhydramine, and an ibuprofen and diphenhydramine combination

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

162

Conditions

Sleep

Interventions

Naproxen Sodium 440 mg (BAYH6689) / DPH 50mgDRUG

Participants received 2 tablets of Naproxen Sodium 220 mg and 2 tablets of Diphenhydramine hydrochloride (DPH) 25 mg, single dose, orally.

Naproxen Sodium 440 mg (BAYH6689)DRUG

Participants received 2 tablets of Naproxen Sodium 220mg and 2 tablets of placebo, single dose, orally.

Naproxen Sodium 220 mg (BAYH6689) / DPH 50mgDRUG

One dose of naproxen sodium 220 mg plus diphenhydramine 50 mg

Eligibility

Sex: ALLMin age: 16 YearsMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Healthy, ambulatory, male and female volunteers between 16-45 years of age; * Scheduled to undergo surgical removal of 1 to 3 impacted third molars, one of which must be at least a partial bony mandibular impaction; * Have moderate to severe postoperative pain on the Categorical Pain Rating Scale and a score of \>/= 50 mm on the 100-mm visual analog Pain Severity Rating Scale by 2030 h +/- 15 minutes on the day of surgery; * Female subjects of childbearing potential must be using a medically acceptable form of birth control for at least 1 month prior to screening (3 months on oral contraceptives), e.g. oral or patch contraceptives, intrauterine device, Depo-Provera, or double-barrier and have a negative pregnancy test at Screening and prior to surgery. Female subjects of nonchildbearing potential must be amenorrheic for at least 2 years or had a hysterectomy and/or bilateral oophorectomy; * Provide a personally signed and dated informed consent indicating that the subject has been informed of all pertinent aspects of the trial, (subjects \<18 years of age must sign a written assent and have parental or guardian consent). Exclusion Criteria: * History of hypersensitivity to naproxen, diphenhydramine, nonsteroidal antiinflammatory drugs (NSAIDS), tramadol, aspirin or any other antihistamine and similar pharmacological agents or components of the products; * Evidence or history of clinically significant (in the judgment of the investigator) hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic diseases, or malignancies within the last 5 years; * Relevant concomitant disease such as asthma (exercise induced asthma is permitted), chronic sinusitis or nasal structural abnormalities causing greater than 50 percent obstruction (polyposis nasi, marked septal deviation) that can interfere with the conduct of the study in the judgment of the investigator; * Current or past history of bleeding disorder(s); * Acute illness or local infection prior to surgery that can interfere with the conduct of the study in the judgment of the investigator; * Chronic use of antihistamines defined as using 5 or more times a week for 2 or more consecutive weeks during the past 3 months; * Positive alcohol breathalyzer test and negative urine drug test prior to surgery; * Females who are pregnant or lactating; * Chronic or severe sleep problems that do not respond to Over the counter (OTC) medication and requires a prescription hypnotic or sedative;

Locations (1)

Unnamed facility

Salt Lake City, Utah, United States

Outcomes

Primary Outcomes

Total Sleep Time Measured by Actigraphy

Actigraphy is a non-intrusive tool that measures an individual's movement during sleep. Actigraphy was used to obtain data in discriminating between sleep and wake states in the subjects. In calculating the total sleep time, subjects who took rescue medication were treated as "awake" from the time the rescue medication was given until the end of the sleep period. In addition, if subjects rescued before sleep onset, their total sleep time was set to zero.

Time frame: Up to 10 hours

Secondary Outcomes

Wake After Sleep Onset (WASO) Measured by Actigraphy

Time frame: Up to 10 hours

Sleep Latency Measured by Actigraphy

Actigraphy is a non-intrusive tool that measures an individual's movement during sleep. Actigraphy was used to obtain data in discriminating between sleep and wake states in the subjects. Sleep latency was defined as minutes to sleep onset since dosing, where sleep onset was the first 20-minute block with 19 minutes of sleep. For subjects who had not achieved sleep onset (e.g., due to taking rescue medication before achieving sleep onset), sleep latency was considered as censored at the time of wakening.

Time frame: Up to 10 hours

Global Assessment of Study Medication as a Sleep-aid

Subject rating of following question with 0 being poor to 4 being excellent: How would you rate the study medication you received as a sleep aid?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Sleep Quality

Data from ClinicalTrials.gov

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Participants received 1 tablet of Naproxen Sodium 220 mg and 3 tablets of placebo, single dose, orally.

DPH 50mgDRUG

Participants received 2 tablets of Diphenhydramine hydrochloride (DPH) 25 mg and 2 tablets of placebo, single dose, orally.

Ibuprofen 400 mg / Diphenhydramine citrate 76 mgDRUG

Participants received 2 tablets of Advil PM (ibuprofen 200 mg and diphenhydramine citrate 38 mg) and 2 tablets of Placebo, single dose, orally.

Subject rating of following question with 1 being very poor and 5 being very good: How was your sleep?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Calmness of Sleep

Subject rating of following question with 1 being very restless and 5 being very calm: How calm was your sleep?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Easiness to Fall Asleep

Subject rating of following question with 1 being very difficult to 5 being very easy: How easy was it to fall asleep?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Premature Awakening

Subject rating of following question with 1 being woke up much too early to 3 being no: Premature awakening?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Ease of Awakening

Subject rating of following question with 1 being very difficult to 5 being very easy: Ease of awakening?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Well Rested

Subject rating of following question with 1 being not rested at all to 3 being completely rested: Well-rested?

Time frame: Up to 10 hours

Karolinska Sleep Diary - Sufficient Sleep

Subject rating of following question with 1 being no, definitely too little to 5 being yes, definitely enough: Did you get enough (sufficient) sleep?

Time frame: Up to 10 hours

Total Sleep Time by Subject Assessment

Subject responded to: Please estimate the number of hours and minutes you think that you slept.

Time frame: Up to 10 hours

Sleep Quality Index

Sleep Quality Index is the mean score of items, 'sleep quality', 'calm sleep', 'ease falling asleep', and 'slept throughout' on the Karolinska Sleep Diary, ranges from 1 (worst possible) to 5 (best possible).

Time frame: Up to 10 hours

Overall Rating of Severity in Categorical Pain Rating Scale Score

Subject responded to question, 'My pain at this time is' by selecting one of the following choices: no pain (0), mild pain (1), moderate pain (2), or severe pain (3).

Time frame: Up to 10 hours

Change From Baseline in Categorical Pain Rating Scale Score

Subjects responded to question, 'My pain at this time is' with following choices: no pain (0), mild pain (1), moderate pain (2), or severe pain (3). Subjects completed this question at baseline (post-dental surgery) and after sleep period. The following measure is the change in pain rating from baseline.

Time frame: Baseline and up to 10 hours

Overall Rating of Severity in Visual Analog Scale (VAS) Score

Subjects marked a line on a 100-mm scale to indicate the severity of pain they are experiencing from 0 being no pain to 100 being worse possible pain.

Time frame: At 10 hours

Change From Baseline in Visual Analog Scale (VAS) Score

Subjects completed the VAS scale at baseline (post-dental surgery) and after completion of the sleep period. Subjects marked a line on a 100-mm scale to indicate the severity of pain they are experiencing from 0 being no pain to 100 being worse possible pain.This measure indicates the change in pain severity rating on the VAS scale from baseline.

Time frame: Baseline and up to 10 hours

Overall Rating of Pain Relief

Subjects responded to question, "Overall, the relief from my starting pain was" by checking one of the following choices: no relief (0), a little relief (1), some relief (2), a lot of relief (3), complete relief (4).

Time frame: Up to 10 hours

Time to Rescue Medication

Subjects were allowed to "rescue" and take a non-study pain reliever if the pain was not tolerable. This measure represents for the time to taking rescue medication from the time the subject took study treatment.

Time frame: Up to 10 hours

Cumulative Proportion of Participants Taking Rescue Medication by Hour

Subjects were allowed to "rescue" and take a non-study pain reliever if the pain was not tolerable. This measure represents for the proportion of subjects who rescued in the study.

Time frame: Up to 10 hours

Global Assessment of Study Medication as a Pain Reliever

Subject responded to question, 'How would you rating this study medication you received as a pain-reliever?' with the following choices: Poor (0), Fair(1), Good(2), Very Good(3), Excellent(4)

Time frame: Up to 10 hours

Number of Times Participants Took Rescue Medication

Subjects were allowed to "rescue" and take a non-study pain reliever if the pain was not tolerable. This measure represents for the number of times rescue medication was taken by a subject.

Time frame: Up to 10 hours

Total Wake Time Measured by Actigraphy

Actigraphy is a non-intrusive tool that measures an individual's movement during sleep. Actigraphy was used to obtain data in discriminating between sleep and wake states in the subjects.

Time frame: Up to 10 hours

Sleep Efficiency Measured by Actigraphy

Sleep efficiency was calculated as (total sleep time/total time in-bed time) × 100; total in-bed time was fixed at 10 hours. Actigraphy is a non-intrusive tool that measures an individual's movement during sleep. Actigraphy was used to obtain data in discriminating between sleep and wake states in the subjects.

Time frame: Up to 10 hours

Activity Mean Measured by Actigraphy

Time frame: Up to 10 hours

Wake Episode Measured by Actigraphy

Actigraphy is a non-intrusive tool that measures an individual's movement during sleep. Actigraphy was used to obtain data in discriminating between sleep and wake states in the subjects. Wake Episodes - # of blocks of continuous wake epochs (defined as 2 or more consecutive epochs scored as wake that ends when there is at least one epoch scored as sleep subsequent to the start of the wake epochs).

Time frame: Up to 10 hours