Intraoperative Superior Hypogastric Plexus Block For Pain Relief During Cesarean-Section

NCT03460093 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2019-03-19

No results posted yet for this study

Summary

PURPOSE: to evaluate the efficacy of superior hypogastric plexus block for pain relief after cesarean section

Conditions

  • Superior Hypogastric Plexus Block

Sponsors & Collaborators

  • Kocaeli Derince Education and Research Hospital

    lead OTHER

Principal Investigators

  • bahar sarıibrahim astepe, M.D · S.B.U Kocaeli Derince Education and Research Hospital

Eligibility

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

Timeline & Regulatory

Start
2018-03-15
Primary Completion
2019-03-15
Completion
2019-03-15

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT03460093 on ClinicalTrials.gov