Fentanyl 12 Mcg Transdermal Patch For Postoperative Pain

The Effect Of Fentanyl 12 Mcg Transdermal Patch On Postoperative Pain Following Unilateral, Single-Level Laminectomy/Discectomy: A Randomized, Controlled, Double-Blind Study

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03199157

Enrollment

Registered

2017-06-26

Start date

2015-03-31

Completion date

2016-12-31

Last updated

2017-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Brief summary

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.

Interventions

DRUGFentanyl transdermal patch

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

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE (Caregiver, Investigator)

Eligibility

Sex/Gender

ALL

Age

20 Years to 70 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame
Numeric rating score for pain (NRS)	Postoperative 24 hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026