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Comparison of misoprostol and hypotensive anesthesia on blood loss during myomectomy

Comparison of misoprostol and hypotensive anesthesia on blood loss during myomectomy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220930056059N1
Enrollment
94
Registered
2022-11-13
Start date
2022-11-11
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

leiomyoma of uterus. Intramural leiomyoma of uterus

Interventions

Intervention 1: Intervention group:In the first group, the bleeding control method is with hypotensive anesthesia. In this group, the average arterial pressure is set to 30% lower than the average art

Sponsors

Vice chancellor for Research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 48 Years

Inclusion criteria

Inclusion criteria: Ages 18-48 Willingness to enter the study Having an indication for abdominal myomectomy

Exclusion criteria

Exclusion criteria: Anemia (hemoglobin less than 10) Allergy to misoprostol Cardiac and pulmonary diseases Use of anticoagulant drugs

Design outcomes

Primary

MeasureTime frame
Blood loss during surgery. Timepoint: During and after surgery. Method of measurement: Volume of blood in suction & bloody sponge count.

Secondary

MeasureTime frame
Vital Signs. Timepoint: Before the intervention, then every 15 minutes until the end of the surgery. Method of measurement: Patient monitoring.;Hemoglobin count . Timepoint: Hemoglobin before & 6 houre & 12 houerafter operation. Method of measurement: Blood examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Maryam Vaezi

Tabriz University of Medical Sciences

mva260@yahoo.com+98 41 3551 9161

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026