Comparison of two drugs as an adjuvant to a local anesthetic for post operative pain relief under spinal anesthesia

Comparison Of Effect Of Midazolam Versus Fentanyl As an Adjuvant To Bupivacaine For Post Operative Analgesia In Lower Abdominal Surgeries Under Spinal Anaesthesia

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/01/017078

Enrollment

140

Registered

2019-01-14

Start date

Unknown

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

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Group M: This group of patients will receive 2mg (0.4ml)of midazolam as an adjuvant to 3ml of 0.5% bupivacaine Control Intervention1: group F: This group of patients will receive 20mcg

Eligibility

Inclusion criteria

Inclusion criteria: ASA I & II Age 18 to 60 years of Both Sex

Exclusion criteria

Exclusion criteria: Patients with any contraindication for spinal anesthesia Patients with psychiatric illness or on any antipsychotic Medication Short stature. Allergic to local anesthetic Patients converted to general anesthesia

Design outcomes

Primary

Measure	Time frame
Duration of post-operative pain reliefTimepoint: Assessed at every 30 minutes interval until the first dose of pain killer is given.	—

Secondary

Measure	Time frame
Time to onset of sensory and motor block.Timepoint: This will be assessed only once after spinal anesthesia. The time taken for establishment of sensory and motor block will be noted.	—

Countries

India

Contacts

Public ContactPG Mundwadkar

Sri Venkateshwaraa Medical College Hospital & Research Centre,

p_mundwadkar@rediffmail.com9844007834

Outcome results

None listed

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