Comparison of labour epidural outcome with and without test dose-a randomized control study

Amrita Institute of Medical Sciences0 sites0 target enrollmentTBD

ConditionsHealth Condition 1: O80- Encounter for full-term uncomplicated delivery

Overview

Phase: Phase 3
Intervention: Not specified
Conditions: Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Sponsor: Amrita Institute of Medical Sciences
Status: Not yet recruiting
Last Updated: 4 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

TBD

End Date

TBD

Last Updated

4 years ago

Study Type

Interventional

Investigators

Sponsor

Amrita Institute of Medical Sciences

Eligibility Criteria

Inclusion Criteria

•All consenting parturient of American society of anaesthesiologists, grade 2 having uncomplicated cephalic singleton pregnancy between age group of 18 t0 40 years and desirous of having a labour epidural

Exclusion Criteria

•Patients with hypersensitivity to study drugs, bleeding disorders, decreased platelet counts, sepsis, spinal column deformities and history of spine surgery will be excluded from the study.

Outcomes

Primary Outcomes

Not specified

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