WHO ICTRP trial
Suppository indomethacin and combined indomethacin- acetaminophen for pain after…
IRCT2013042013069N1 · Iranian Registry of Clinical Trials (IRCT) · Not Recruiting
Key facts
| Trial ID | IRCT2013042013069N1 |
|---|---|
| Public title | Suppository indomethacin and combined indomethacin- acetaminophen for pain after cesarean section |
| Scientific title | Comparison of suppository indomethacin and combination of indomethacin- acetaminophen on post operative pain after cesarean section |
| Primary sponsor | Kermanshah University of Medical Sciences, Vice chancellor for research |
| Registry | Iranian Registry of Clinical Trials (IRCT) |
| Recruitment status | Not Recruiting |
| Study type | interventional |
| Phase | 3 |
| Countries | Iran (Islamic Republic of) |
| Conditions | Post-cesarean pain. Delivery by caesarean section, unspecified;Delivery by caesarean section, unspecified |
| Interventions | Intervention 1: Group A: A 50-mg indomethacin rectal suppository is administered immediately after a cesarean every 6 hours for 24 hours after the operation. Intervention 2: Group B: Two rectal suppositories (A 50-mg indomethacin and a… |
| Registration date | Sep 22, 2013 |
| Target size | 76 |
| Registry page | irct.behdasht.gov.ir |
At a glance
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: