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EFFICACY OF INTRATHECAL 0.5% HYBERBARIC BUPIVACAINE 5mg WITH FENTANYL 10mcg VERSUS 0.5% HYPERBARIC BUPIVACAINE 5mg WITH FENTANYL 20mcg ON LEVEL AND DEPTH OF ANAESTHESIA AND HEMODYNAMIC PARAMETERS IN PARTURIENTS UNDERGOING CESAREAN SECTION: A RANDOMISED STUDY

EFFICACY OF INTRATHECAL 0.5% HYBERBARIC BUPIVACAINE 5mg WITH FENTANYL 10mcg VERSUS 0.5% HYPERBARIC BUPIVACAINE 5mg WITH FENTANYL 20mcg ON QUALITY OF ANAESTHESIA AND HEMODYNAMIC PARAMETERS IN PARTURIENTS UNDERGOING CESAREAN SECTION: A RANDOMISED STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036743
Enrollment
100
Registered
2021-09-22
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: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: 0.5% HYPERBARIC BUPIVACAINE 5 mg WITH FENTANYL 10 mcg: INTRATHECAL INJECTION OF 0.5% HYPERBARIC BUPIVACAINE 5 mg WITH FENTANYL 10 mcg, TOTAL VOLUME TO BE MADE 2 ml BY ADDING NORMAL SALI

Sponsors

BANGALORE MEDICAL COLLEGE AND RESEARCH INSTITUTE
Lead Sponsor
DR RAMESH R
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: ASA CLASS II, AGED BETWEEN 18 TO 40 YEARS, POSTED FOR ELECTIVE CESAREAN SECTION

Exclusion criteria

Exclusion criteria: PATIENTS REFUSAL ALLERGIC TO DRUG OBESE ASA CLASS III OR IV PRE ECLAMPSIA, ECLAMPSIA, CARDIAC OR RESPIRATORY INSUFFICIENCY, TWIN GESTATION SEVERE FETAL DISTRESS, PLACENTAL ABRUPTION, PLACENTA PREVIA, CORD PROLAPSE CONTRAINDICATIONS FOR NEURAXIAL BLOCKADE

Design outcomes

Primary

MeasureTime frame
QUALITY OF ANASTHESIA - LEVEL AND DEPTH OF SENSORY AND MOTOR BLOCKADETimepoint: BASELINE READING AND 1MIN AFTER SAB, 2MIN, 3MIN, 5MIN, 10MIN, 15MIN, 20MIN, 25MIN, 30MIN, 40MIN,50MIN, 60MIN, 75MIN, 90MIN, 105MIN, 120MIN, POSTOPERATIVELY HOURLY FOR 4 HOURS—

Secondary

MeasureTime frame
NO HEMODYNAMIC CHANGES OR SIDE EFFECTSTimepoint: BASELINE READING AND 1MIN AFTER SAB, 2MIN, 3MIN, 5MIN, 10MIN, 15MIN, 20MIN, 25MIN, 30MIN, 40MIN,50MIN, 60MIN, 75MIN, 90MIN, 105MIN, 120MIN, POSTOPERATIVELY HOURLY FOR 4 HOURS—

Countries

India

Contacts

Public ContactDR RAMESH R

BANGALORE MEDICAL COLLEGE AND RESEARCH INSTITUTE

rameshrevanna@yahoo.co.in9844837939

Outcome results

None listed

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