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NCT04519593

ABSOLUTELY: A Temporary Uterine Blood Supply Occlusion for Laparoscopic Myomectomy in Patients With UTErine LeiomYoma

Status unknown NA Last updated 14 July 2021
What this trial tests

NA trial testing Laparoscopic myomectomy with prior temporary uterine blood supply occlusion in Uterine Leiomyoma in 120 participants. Status unknown.

Timeline
27 September 2020
Primary endpoint
31 August 2022
1 November 2022

Quick facts

Lead sponsorMother and Child Clinic Saint-Petersburg
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment120
Start date27 September 2020
Primary completion31 August 2022
Estimated completion1 November 2022
Sites1 location across Russia

Drugs / interventions tested

Conditions studied

Sponsor

Mother and Child Clinic Saint-Petersburg

Who can join

18 and older, female only, with Uterine Leiomyoma or Uterine Fibroid. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A phase 3 multicenter unblinded randomized controlled trial comparing the temporary uterine blood supply occlusion with conventional approach during laparoscopic myomectomy in patients with uterine leiomyoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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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/NCT04519593.

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