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A clinical study to compare the pain relief among two drugs in spinal anaesthesia for cesarean section.

Comparison Of Fentanyl With Midazolam as an adjuvant to Levobupivacaine for spinal Anaesthesia in Cesarean Section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049315
Enrollment
90
Registered
2023-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Spinal fentanyl: Duration is for first 24 hours postoperatively Control Intervention1: Spinal Midazolam: Duration is for first 24 hours postoperatively

Sponsors

SRM Medical college Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA II who were scheduled for elective cesarean section 2. Single intrauterine gestation.

Exclusion criteria

Exclusion criteria: 1.Significant cardiovascular or hepatorenal diseases. 2.Altered mental status , deranged coagulation profile. 3.Patients receiving antiemetics 24 hours prior. 4.Contraindication to central neuraxial blockade. 5.Hypersensitivity to study drug

Design outcomes

Primary

MeasureTime frame
To compare the duration of postoperative analgesia Timepoint: Immediately after surgery till 24hours—

Secondary

MeasureTime frame
Duration of sensory and motor blockade Timepoint: Immediately after surgery;Incidence of nausea and vomitingTimepoint: After surgery till 24hours;Onset of sensory blockade. Timepoint: Immediately after spinal anaesthesia—

Countries

India

Contacts

Public ContactYazhini

Srm Medical College Hospital and Research Institute

drvenkat94@gmail.com9894581455

Outcome results

None listed

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