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How a spinal pain medication helps control blood pressure during surgery on the uterus : a study

The effect of intrathecal clonidine on hypertensive response to intramyometrial vasopressin during myomectomy- RCT. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073630
Enrollment
48
Registered
2024-09-09
Start date
Unknown
Completion date
Unknown
Last updated
2024-09-16

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: D259- Leiomyoma of uterus, unspecified

Interventions

Intervention1: Intrathecal Clonidine with Bupivacaine: In patients undergoing open myomectomy we will give intrathecal clonidine with bupivacaine before starting surgery to provide anaesthesia. In thi

Sponsors

Jawaharlalal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient age between 18-50 years ASA physical status 1 and 2 Patients requiring intra myometrial Vasopressin injection

Exclusion criteria

Exclusion criteria: H/O allergy to study drugs (Local anesthetics, Vasopressin and Clonidine). Pre-existing arrythmia, Heart block and structural heart disease. Any contraindications for spinal anesthesia. Short stature (Height BMI > 30kg/m2 Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To compare hypertensive response (defined as mean arterial pressure more than or equal to 10 mm of Hg from the baseline value within 60 minutes of intramyometrial vasopressin injection between study and control group.Timepoint: Every minute for first 20 minutes after intramyometrial vasopressin injection , every 5 minutes there after till 60 minutes

Secondary

MeasureTime frame
To compare systolic and diastolic blood pressure between groups To compare heart rate between groups To compare side effects like sedation, dry mouth, bradycardia or tachycardia episodes Postoperative motor and sensory regression time First dose analgesia requirement timeTimepoint: upto 24 hours following surgery

Countries

India

Contacts

Public ContactDr Sakthirajan P

Jawaharlal Institute of Postgraduate Medical Education and Research

sakthiab8@gmail.com8903468132

Outcome results

None listed

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