Epidural Catheter and Surgically Implanted Rectus Sheath Catheter in Management of Postoperative Pain

Menoufia University120 enrolled

Overview

One hundred and twenty patients at age range from 18 to 60 undergoing laparotomy was enrolled in this study. Patients were randomly assigned to two groups 60 in epidural group and the other 60 patients in rectus catheter group. epidural catheter inserted pre induction but rectus sheath catheter inserted by the surgeon at the end of surgery. In both groups we activated with10 ml bupivacain25% before patient recovery then 10 ml bupivacain.125% each 6 hours. If patient still in pain 1gm perflgan injected. If patient still in pain 10 mg nalufine for 70 kg patient injected. we will record pulse, blood pressure and visual analogue scale at 0,6,12,24 and 36 hours postoperative. Also Occurrence of nausea and vomiting, Time of return of bowel movement, Time of discharage and amount of analgesia used will be recorded. Results, discution will be later.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

SINGLE

Enrollment

120

Conditions

Postoperative Pain

Interventions

Epidural catheterDEVICE

epidural catheter inserted pre induction

rectus sheath catheterDEVICE

The surgeon will place one hand inside the abdomen and with the other hand inserted the Tuohy needle through the skin and fascia. The surgeon will feel when the needle tip is just superfacial to interface between the peritoneum and muscle layer and avoid penetration of inferior epigastric artery. The procedure will be repeated on the contralateral

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: * patients at age rang from 18 to 60 undergoing laparotomy * patients ASA1,2 physical status Exclusion Criteria: * any known coagulopathy * morbid obesity * kyphosis or scoliosis * those with known sensitivity to local anesthetic drugs * lack of cooperation and inability to understand or perform verbal or physical assessments.

Locations (2)

Faculty of Medicine Menoufia University

Cairo, Governorate, Egypt

Menoufia University

Cairo, Governorate, Egypt

Outcomes

Primary Outcomes

Postoperative pain relief

Measured by Visual Analogue Scale (VAS) pain measurement scale divided from 0 to 10 where 0 is no pain and10 worst pain can be imagined

Time frame: 36hours

Secondary Outcomes

Side effects

Occurrence any side effects Time of return of bowel movement. Time of discharage. Amount of analgesia used

Time frame: 36hours

Total of analgesic consumption

total consumption of naluphine and paracetamol pre milligram

Time frame: 36 hours

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.