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NCT05622656
Dexmedetomidine Reduce Postoperative Pain of C-section
Phase 4 trial testing Dexmedetomidine in Pain, Postoperative in 80 participants. Status unknown.
31 March 2023
Quick facts
| Lead sponsor | First People's Hospital of Chenzhou |
|---|---|
| Phase | Phase 4 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | prevention |
| Enrollment | 80 |
| Start date | 1 December 2022 |
| Primary completion | 31 March 2023 |
| Estimated completion | 31 March 2023 |
| Sites | 1 location across China |
Drugs / interventions tested
- Dexmedetomidine (dexmedetomidine) — full drug profile →
- Placebo
Conditions studied
- Pain, Postoperative — all drugs for Pain, Postoperative →
Sponsor
First People's Hospital of Chenzhou
Who can join
Adults 18 to 50, female only, with Pain, Postoperative. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study was to make sure whether the infiltration of dexmedetomidine around the uterus can reduce the pain of cesarean section surgery.Studies have shown that the use of local anesthetic infiltration around the uterus can reduce pain after cesarean section surgery.In observed group, 50ug of dexmedetomidine (volume 10ml) was infiltrated around the uterus at the end of the caesarean section, while in controled group, 10ml normal saline as placebo was infiltrated around the uterus. VASs was accessed in 2h 12h,24h,48h after surgery.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT05622656
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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- NCT07377981 — An Exploratory Study of the Efficacy and Safety of Esketamine and Dexmedetomidine in Non-Intubated ICU Patients With Hyp · Phase 4 · not yet recruiting
- NCT07306702 — Dexmedetomidine-Enhanced PCIA After Lobectomy in Nicotine-Dependent Patients · Phase 4 · withdrawn
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Other recruiting trials for Pain, Postoperative
Currently open trials in the same condition.
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Other First People's Hospital of Chenzhou trials
Trials by the same sponsor.
- NCT06237751 — Preoperative Sildenafil Administration for Hepatectomy · NA · recruiting
- NCT06254092 — Effect of Tourniquet Binding of Cervical on the Blood Volume of Amniotic Fluid in Cesarean Section · NA · unknown
- NCT05735132 — Novel Local Infiltration Anesthesia for Radial Artery Cannulation. · NA · unknown
- NCT05644535 — Cerebrospinal Fluid Gravity Correlation Analysis · unknown
- NCT04555980 — Warm Patch Decrease Propofol Injection Pain · NA · completed
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 NCT05622656 (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 First People's Hospital of Chenzhou
- Last refreshed: 18 November 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/NCT05622656.
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