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Effect of tapontadol and oxycodone in pain control

Effect of premedication with Tapentadol and Oxycodone sustain release for post operative pain control in Laparascopic cholecystectomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190618043923N2
Enrollment
60
Registered
2019-07-08
Start date
2019-08-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Patients with calculus of gallbladder candidated for laparoscopic cholecystectomy. Calculus of gallbladder without cholecystitis

Interventions

Intervention 1: Intervention group 1: Receiving Pre-treatment regimens of one oral tablet of tapentadol 75 mg (NUCYNTA) branded by Collegium Pharmaceutical, Inc., an hour before surgery, with naproxe

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with cholelithiasis undergoing elective laparoscopic cholecystectomy Physical status 1 or 2 according to the classification of the American Association of Anesthesiologists

Exclusion criteria

Exclusion criteria: Sensitivity to tapontadol or oxycodone History of chronic consumption of other opioids or analgesics Cardiac, liver, respiratory or renal disease Surgeries for over one and a half hours Complicated surgeries

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: Measuring the pain intensity at the beginning of the study (after surgery) and every two hours after the operation for up to 12 hours. Method of measurement: Visual analogue scale.;First request for pain medication. Timepoint: From the beginning of the study (after surgery) up to 12 hours after surgery. Method of measurement: Check patient records.;Amount of pain medication within 12 hours after surgery. Timepoint: From the beginning of the study (after surgery) up to 12 hours after surgery. Method of measurement: Check patient records.;Pain duration. Timepoint: From the beginning of the study (after surgery) up to 12 hours after surgery. Method of measurement: Self-declaration.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDawood Aghamohammadi

Tabriz University of Medical Sciences

daghamohamadi@yahoo.com+98 984133361928

Outcome results

None listed

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