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NCT03636048

Comparison of Anesthesia Type in Patients Undergoing Transabdominal Cervico Isthmic Cerclage (TCIC)

Terminated NA Last updated 4 September 2020
What this trial tests

NA trial testing Bupivacaine Hcl 0.5% Inj in Cervical Incompetence in 20 participants. Terminated before completion.

Timeline
1 August 2018
Primary endpoint
1 June 2020
1 June 2020

Quick facts

Lead sponsorHallym University Kangnam Sacred Heart Hospital
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment20
Start date1 August 2018
Primary completion1 June 2020
Estimated completion1 June 2020
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Hallym University Kangnam Sacred Heart Hospital

Who can join

Adults 20 to 50, female only, with Cervical Incompetence. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The investigator aimed to compare the effect of anesthesia on overall postoperative outcomes including post-operative pain score and the fetal well-being (heart rate) in patients undergoing transabdominal cervico isthmic cerclage(TCIC). The investigator divided the patients into two groups. The first group was the patients who undergo general anesthesia with postoperative wound patient-controlled analgesia device(PCA) and the second group was the patients who undergo combined spinal-epidural anesthesia(CSE) with postoperative epidural catheter PCA device for pain control.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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