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NCT03382938

Dexmedetomidine Wound Infiltration in Cesarean Section

Recruiting now NA Last updated 19 March 2025
What this trial tests

NA trial testing Dexmedetomidine in Postoperative Pain in 100 participants. Currently enrolling.

Timeline
23 August 2019
Primary endpoint
20 December 2025
20 November 2026

Quick facts

Lead sponsorAttikon Hospital
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposeprevention
Enrollment100
Start date23 August 2019
Primary completion20 December 2025
Estimated completion20 November 2026
Sites1 location across Greece

Drugs / interventions tested

Conditions studied

Sponsor

Attikon Hospital

Who can join

Adults 18 to 40, female only, with Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The effects of four different wound infiltration protocols in cesarean section will be investigated on parturient' pain intensity, PCA morphine consumption given, side effects and parturient' overall satisfaction. One group will receive for wound infiltration dexmedetomidine, the second ropivacaine, the third dexmedetomidine combined with ropivacaine, while the last one will receive normal saline (placebo group).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of Dexmedetomidine

Trials testing the same drug.

Other recruiting trials for Postoperative Pain

Currently open trials in the same condition.

Other Attikon Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT03382938.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing