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Comparison of different doses of Oxytocin during caesarian delivery

Comparison of efficacy and safety of two different doses of Oxytocin during caesarian delivery - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054979
Enrollment
75
Registered
2023-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

None listed

Interventions

Intervention1: J RADHA: HEAD OF THE DEPARTMENT DEPARTMENT OF ANAESTHESIOLOGY S V MEDICAL COLLEGE TIRUPATI

Sponsors

medical Superintendent
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) ASA PS I and II 2) Aged between 18 to 40 years 3) Elective Cesarean section under Spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1. Previous history of oxytocin allergy 2. Valvular diseases complicating pregnancy 3. Other cardiac diseases complicating pregnancy

Design outcomes

Primary

MeasureTime frame
Comparison of efficacy & safety of two different doses of Oxytocin during caesarean deliveryTimepoint: 4—

Secondary

MeasureTime frame
Adequacy of uterine contractions Haemodynamic changes 3. Requirement of additional uterotonic agents. 4. Adverse effectsObjectives: To compare the following parameters between two different doses of oxytocin Timepoint: 4—

Countries

India

Contacts

Public ContactMohana Krishna Reddy Egabojjireddygari

sri venkateswara Medical college

mkreddydoctor@gmail.com7013558161

Outcome results

None listed

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