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Spinal Anesthesia and General Anesthesia for Pyloromyotomy - Surgical Outcomes a Comparison Retrospective Study

NCT03095144 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2017-03-29

No results posted yet for this study

Summary

Background: The purpose of this retrospective study is to evaluate surgical outcomes of pyloromyotomy in infants performed under spinal anesthesia compares to general anesthesia.

Methods: After receiving the approval of the hospital ethics committee, retrieving, reviewing files and collecting data. Primary outcomes: total operating room time, duration of surgery, pain management and postoperative apnea episodes, time of regaining full enteral feeding. Secondary outcome measures: include cardio-respiratory changes and events, and substantial vomiting postoperatively.

Conditions

  • Hypertrophic Pyloric Stenosis
  • Spinal Anesthesia
  • General Anesthesia

Interventions

DEVICE

Spinal anesthesia

Pyloromyotomy under spinal anesthesia

DEVICE

General anesthesia

Pyloromyotomy under general anesthesia

Sponsors & Collaborators

  • Bnai Zion Medical Center

    lead OTHER_GOV

Principal Investigators

  • Mostafa Somri, Prof · Bnai Zion Medical Center

Eligibility

Min Age
4 Weeks
Max Age
6 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-31
Primary Completion
2017-07-31
Completion
2017-12-31
FDA Device
Yes

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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 NCT03095144 on ClinicalTrials.gov