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COMPARING PSYCHOMOTOR RECOVERY AFTER GIVING TWO DIFFERENT DRUGS FOR SEDATION DURING SPINAL ANAESTHESIA

PSYCHOMOTOR RECOVERY OF DEXMEDETOMIDINE COMPARED WITH PROPOFOL AFTER SEDATION DURING SPINAL ANAESTHESIA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/02/007953
Enrollment
66
Registered
2017-02-22
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: - Health Condition 2: 3- Administration Health Condition 3: null- ASA 1,2 PATIENTS

Interventions

Intervention1: dexmedetomidine: spinal anesthesia will be performed with 0.5% bupivacaine 3cc.group D will receive sedative doses of dexmedetomidine of 0.5 microgarm/kg IV loading dose for 15 minutes

Sponsors

JIPMER INSTITUTE
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 ASA class I &II 2 Age between 18 to 60 years of either sex 3 Patients scheduled for elective lower abdominal urological gynecological and orthopaedic surgeries under spinal anaesthesia

Exclusion criteria

Exclusion criteria: 1 Any contra-indication to sub arachnoid block like hypotension coagulation defects spine abnormalities etc 2 BMI more than 30 height less than 150cm for males height less than 140cm for females 3 Patients with known allergies to any of the test drugs 4 Pregnancy 5 Patients with cognitive deficits pre existing depression

Design outcomes

Primary

MeasureTime frame
1. To evaluate the psychomotor recovery after sedation with dexmedetomidineTimepoint: 1 YEAR 6 MONTHS—

Secondary

MeasureTime frame
2. To compare with propofol during spinal anaesthesiaTimepoint: 1 YEAR 6 MONTHS—

Countries

India

Contacts

Public ContactTILAK PERIKA

JIPMER, Pondicherry

sumanlata13@yahoo.com09585318277

Outcome results

None listed

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