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NCT04801277

Efficacy of PC6 Electroacupuncture in the Prevention of Nausea Vomiting in Caesarean Patient Under Spinal Anaesthesia

Status unknown NA Last updated 16 March 2021
What this trial tests

NA trial testing Electroacupuncture on acupoints vs sham points in Postoperative Nausea and Vomiting in 100 participants. Status unknown.

Timeline
1 September 2020
Primary endpoint
31 March 2021
30 April 2021

Quick facts

Lead sponsorClinical Research Centre, Malaysia
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment100
Start date1 September 2020
Primary completion31 March 2021
Estimated completion30 April 2021
Sites1 location across Malaysia

Drugs / interventions tested

Conditions studied

Sponsor

Clinical Research Centre, Malaysia

Who can join

Adults 18 to 45, female only, with Postoperative Nausea and Vomiting. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To determine the ability of electroacupuncture on PC6 versus sham acupuncture in reducing incidence of intraoperative and postoperative nausea vomiting in parturients who underwent Caesarean delivery under spinal anaesthesia

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Postoperative Nausea and Vomiting

Currently open trials in the same condition.

Other Clinical Research Centre, Malaysia 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/NCT04801277.

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