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Intrathecal Analgesia for Normal Labour

NCT04221568 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2020-01-09

No results posted yet for this study

Summary

Primary outcome: Compare the duration of analgesia. Secondary outcome: analgesic potency of bupivacaine and fentanyl versus levobupivacaine and fentanyl.

Conditions

  • Labor Pain

Interventions

DRUG

Bupivacaine-fentanyl

local anathetic\&analgesic drugs

DRUG

levobupivacaine-fentanyl

local anathetic\&analgesic drugs

Sponsors & Collaborators

  • Assiut University

    lead OTHER

Principal Investigators

  • hamdy abbas · Assiut University

  • wesam nashat · Assiut University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-03-01
Primary Completion
2021-03-01
Completion
2021-03-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04221568 on ClinicalTrials.gov