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NCT04068766: PALM

Efficacy of Paracervical Block in Laparoscopic Myomectomy: a Randomized Controlled Trial (PALM)

Status unknown NA Last updated 28 August 2019
What this trial tests

NA trial testing Paracervical block in Uterine Fibroid in 62 participants. Status unknown.

Timeline
23 August 2019
Primary endpoint
1 August 2020
1 August 2020

Quick facts

Lead sponsorKangbuk Samsung Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment62
Start date23 August 2019
Primary completion1 August 2020
Estimated completion1 August 2020
Sites2 locations across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Kangbuk Samsung Hospital

Who can join

Adults 18 to 60, female only, with Uterine Fibroid. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

It remains controversial whether paracervical block should be performed as a powerful strategy for pain relief in laparoscopic myomectomy (LM), because convincing conclusions are difficult to draw because of the heterogeneous and contradictory nature of the literature. Therefore, the aim of this study was to evaluate the efficacy of paracervical blocks using with 0.5% bupivacaine prior to LM for benign gynecologic conditions on postoperative pain relief.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Paracervical block

Trials testing the same drug.

Other recruiting trials for Uterine Fibroid

Currently open trials in the same condition.

Other Kangbuk Samsung 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/NCT04068766.

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