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Comparison between effect of two drugs on blood loss in patients undergoing abdominal myomectomy operation

Effect of Oxytocin and Carbetocin infusion on blood loss during abdominal myomectomy– a comparative study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061949
Enrollment
52
Registered
2024-01-29
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: D259- Leiomyoma of uterus, unspecified Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Carbetocin infusion: To determine the intra-operative blood loss during elective abdominal myomectomy under sub-arachnoid block in patients to whom pre-operative Carbetocin infusion is

Sponsors

Institute of Post Graduate Medical Education and Research and SSKM Hospital Kolkata
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Body weight between 50 - 90 kgs 2. Symptomatic leiomyomas and scheduled to undergo abdominal myomectomy 3. With number of myoma = 5 4. Myoma FIGO staging 3 to 6

Exclusion criteria

Exclusion criteria: 1. Unwilling patient 2. Patients undergone vaginal or laparoscopic myomectomy 3. Patients received preoperative embolisation or GnRh analogue 4. Previous myomectomy 5. Pregnant and postmenopausal women 6. Myoma FIGO staging 1,2,7 & 8 7. Cervical and broad ligament myoma 8. Allergy or contraindications to Carbetocin such as coronary artery disease, asthma, epilepsy, migraine, kidney and hepatic diseases 9. Preoperative haemoglobin concentration less than 10 gm per dL

Design outcomes

Primary

MeasureTime frame
Estimated intra-operative blood loss (mL)Timepoint: Intra-operative period

Secondary

MeasureTime frame
1. Need for intraoperative and postoperative blood transfusion 2. Preoperative and postoperative haemoglobin values (measured after 6 and 24 hours of surgery) 3. Operative time 4. Duration of postoperative hospital stay 5. Drug-related adverse effects 6. Operative complications.Timepoint: Intra-operative period and Post-operative period

Countries

India

Contacts

Public ContactDr Soma Chakraborty

Institute of Post Graduate Medical Education and Research (IPGME&R) and SSKM Hospital, Kolkata

drsoma.chakraborty@gmail.com9547032006

Outcome results

None listed

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