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Fixed Combination of Dipyrone and Codeine for Controlling Pain After Pelvic-abdominal Surgery

NCT04641338 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 491

Last updated 2026-05-11

No results posted yet for this study

Summary

Phase III clinical trial, multicentre, superiority, randomized, open, parallel groups, with active control and use of postoperative oral medication (multiple doses of medication).

Conditions

  • Pain, Postoperative

Interventions

DRUG

Fixed dose combination Dipyrone and Codeine

Fixed dose combination: dipyrone 1000 mg + codeine 30 mg every 6 hours

DRUG

Dipyrone

use of 1000 mg dipyrone every 6 hours

DRUG

Codeine

30 mg codeine every 6 hours.

Sponsors & Collaborators

  • Brainfarma Industria Química e Farmacêutica S/A

    collaborator INDUSTRY

  • Brazilian Clinical Research Institute

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-03-16
Primary Completion
2024-03-15
Completion
2024-05-17

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04641338 on ClinicalTrials.gov