Fentanyl 12 Mcg Transdermal Patch For Postoperative Pain

Phase 4CompletedNCT03199157

Baskent University78 enrolled

Overview

The investigators designed a prospective randomized study to investigate the effect of fentanyl 12 mcg transdermal patch on postoperative pain following unilateral, single-level laminectomy/discectomy.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Postoperative Pain

Interventions

Fentanyl transdermal patchDRUG

Patients received fentanyl 12 mcg transdermal patch group 8 hours preoperatively and until 24 hours after the surgery

Eligibility

Sex: ALLMin age: 20 YearsMax age: 70 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients between the ages of 20-70 years * ASA physical status 1-2 patients undergoing single-level laminectomy/discectomy Exclusion Criteria: * A history of allergy to any study drugs * History of opioid use, obstructive sleep apnea * Any psychological disorders * hepatic or renal failure

Outcomes

Primary Outcomes

Numeric rating score for pain (NRS)

Time frame: Postoperative 24 hours

Data from ClinicalTrials.gov

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