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Comparison Between Sublingual Buprenorphine and Fentanyl Intravenous Pump for Postoprative Pain Relief After Open Cholecystectomy Surgery.

Comparison Between Sublingual Buprenorphine and Fentanyl Intravenous Pump for Postoprative Pain Relief After Open Cholecystectomy Surgery.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190901044665N1
Enrollment
80
Registered
2019-10-30
Start date
2019-06-22
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Comparison between Sublingual Buprenorphine and Fentanyl Intravenous Pump for postoperative pain relief after open Cholecystectomy Surgery.

Interventions

Intervention 1: In the intervention group, Sublingual Buprenorphine Tablet administered 0.4 mg in 6, 12 and 18 hours recovey and Placebo Pump 50 cc normal saline in recovery and continued for 24 hour

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients undergoing open cholecystectomy Patients ASA 1and2 Patients who have no further surgery Age range 20 to 50 years

Exclusion criteria

Exclusion criteria: History of opium use Nervous drug history Active asthma ASA3 Other concurrent surgery Surgery lasted Complicated surgery

Design outcomes

Primary

MeasureTime frame
Reduction of pain after open Cholecystectomy. Timepoint: VRS score(Verbal Rating Score) in both groups at the time of study (in recovery,2,6,12,18 and 24) will be evaluated. Method of measurement: Through the Score Verbal Rating Scale (VRS).

Secondary

MeasureTime frame
Nausea and Vomiting Score after open Cholecystectomy. Timepoint: Nausea and Vomiting in both groups at the time of study (in recovery,2,6,12,18 and 24) will be evaluated. Method of measurement: By Scoring N&V Score.;Sedation Score after open Cholecystectomy. Timepoint: Sedation Score(Through the Ramsay relaxation Scale) in both groups at the time of study (in recovery,2,6,12,18 and 24) will be evaluated. Method of measurement: Through the Ramsay relaxation Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAhmad Ghazi

Ardabil University of Medical Sciences

dr.ghaziahmad@gmail.com009844838649

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026