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Comparison of 3 Different Density Levobupivacaine Solutions + Fentanyl for Spinal Anaesthesia for Caesarean Delivery.

NCT03956303 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2019-05-20

No results posted yet for this study

Summary

The investigator's aim is to compare the efficacy of 3 levobupivacaine solutions with different density on spinal anesthesia for caesarean delivery.

Conditions

  • Anesthesia

Interventions

DRUG

Chirocaine %0.5

Levobupivacaine 8 mg Chirocaine (% 0.5) +20 mcg fentanyl

DRUG

Chirocaine Heavy 40

Chirocaine (%0.75) + Dextrose 40 mg+20 mcg fentanyl

DRUG

Chirocaine Heavy 60

Chirocaine (%0.75) + Dextrose 60 mg+20 mcg fentanyl

DRUG

Chirocaine Heavy 80

Chirocaine (%0.75) + Dextrose 80 mg+20 mcg fentanyl

Sponsors & Collaborators

  • Balikesir University

    lead OTHER

Principal Investigators

  • Ozlem Sagir, Assist. Prof · Balikesir University School of Medicine Department of Anesthesia and Reanimation

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2016-06-30
Completion
2016-08-31

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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 NCT03956303 on ClinicalTrials.gov