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A clinical study on the effect of glycopyrrolate on the maternal blood pressure and vasopressor requirement during cesarean delivery

The effect of prophylactic intravenous glycopyrrolate on the incidence of hypotension and vasopressor requirement during spinal anaesthesia for caesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/12/029495
Enrollment
60
Registered
2020-12-02
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: Glycopyrrolate, normal saline as control agent: Intravenous Glycopyrrolate 0.2mg given to patients undergoing cesarean delivery under spinal anesthesia. Control Intervention1: Normal

Sponsors

JSS Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Height- 150-170cm Body mass index Singleton pregnancy

Exclusion criteria

Exclusion criteria: Patients having contraindications to spinal anaesthesia i.e, patient refusal, local infection, allergy to local anaesthetics, bleeding disorders, spinal deformity, severe congenital or acquired heart disease, hemorrhage or hypovolemic shock (each condition ruled out via good history, clinical examination, & or investigations) Known sensitivity to the study drugs

Design outcomes

Primary

MeasureTime frame
The incidence of hypotension and vasopressor requirement during spinal anaesthesia for cesarean deliveryTimepoint: Hypotension is assessed from 1 minute after administration of spinal anaesthesia up to 60 minutes or end of surgery whichever is the earliest. Total amount IV Ephedrine 6mg given intra-operative period from 1 minute of spinal-anaesthesia administration up to the end of surgery.

Secondary

MeasureTime frame
Incidence of bradycardia and requirement of atropine Incidence of nausea, vomiting and dryness of mouth. Time for onset , maximum level and duration of sensory block Time for 2 segment regression of sensory block Time for onset of motor block, maximum level and duration of motor block APGAR score Timepoint: Bradycardia below 60 beats/min. Effect of spinal anesthesia on motor and sensory blockade.

Countries

India

Contacts

Public ContactDr Gurudatt C L

JSS MEDICAL COLLEGE AND HOSPITAL

dattguru55@gmail.com9845312311

Outcome results

None listed

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