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NCT05021315
Vaginal Cleaning Using Povidone Iodine Before CS to Reduce Postoperative Wound Infection
Phase 3 trial testing 10% povidone iodine in Cesarean Section Complications in 800 participants. Status unknown.
30 September 2022
Quick facts
| Lead sponsor | Cairo University |
|---|---|
| Phase | Phase 3 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 800 |
| Start date | 15 September 2021 |
| Primary completion | 30 September 2022 |
| Estimated completion | 15 October 2022 |
| Sites | 2 locations across Egypt |
Drugs / interventions tested
- 10% povidone iodine — full drug profile →
Conditions studied
- Cesarean Section Complications — all drugs for Cesarean Section Complications →
- Vaginal Infection — all drugs for Vaginal Infection →
- Postoperative Infection — all drugs for Postoperative Infection →
Sponsor
Cairo University
Who can join
Adults 18 to 38, female only, with Cesarean Section Complications or Vaginal Infection. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of work to assess the effectiveness of preoperative vaginal cleansing with povidone iodine on reduction of post caesarean section wound infection Research questions: Does vaginal cleaning using povidone iodine before cesarean section has effect on reduction of postoperative wound infection??
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05021315
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of 10% povidone iodine
Trials testing the same drug.
- NCT05896462 — Effect of Skin Antisepsis After Skin Closure on Wound Infection After Abdominal Surgery for Sepsis: a Preliminary Report · NA · completed
Other recruiting trials for Cesarean Section Complications
Currently open trials in the same condition.
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- NCT07130747 — Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section · NA · recruiting
- NCT05791630 — The Norwegian World Health Organisation Labour Care Guide Trial (NORWEL) · NA · recruiting
- NCT07049705 — Factors Influencing Bradycardia During Spinal Anesthesia in Obstetric Patients Undergoing Cesarean Section · active not recruiting
Other Cairo University trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05021315 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Cairo University
- Last refreshed: 18 July 2022
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05021315.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing