Completed PHASE2 INTERVENTIONAL 2-arm NCT03041779

Comparison Between Rectal Suppository Acetaminophen and Diclofenac Sodium as Analgesia for Postpartum Perineal Tear (SuPPerP)

A Single Blinded, Open-labelled, Randomized Control Trial Comparing Acetaminophen Rectal Suppository With Diclofenac Rectal Suppository as Analgesia for Perineal Injury Following Childbirth

Sponsor: Clinical Research Centre, Malaysia

Conditions Perineal Laceration (Obstetric) Perineal Tear

Interventions Diclofenac Sodium 50Mg Suppository Paracetamol 500Mg Suppository

Updated 5 times since 2017 Last updated: Feb 1, 2017 Started: Oct 31, 2015 Primary completion: Jul 31, 2016 Completion: Jul 31, 2016

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE2 clinical study on Perineal Laceration (Obstetric) and Perineal Tear, this trial is completed. The trial is conducted by Clinical Research Centre, Malaysia and has accumulated 5 data snapshots since 2015. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.

Status Flow

Change History

5 versions recorded

Sep 2024 — Present [monthly]

Completed PHASE2
Jul 2024 — Sep 2024 [monthly]

Completed PHASE2
Jan 2021 — Jul 2024 [monthly]

Completed PHASE2
Jun 2018 — Jan 2021 [monthly]

Completed PHASE2
Feb 2017 — Jun 2018 [monthly]

Completed PHASE2

First recorded

Oct 2015

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Clinical Research Centre, Malaysia

Data source: Clinical Research Centre, Malaysia

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

No location information available.