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Comparing Two Types of Sedation to Gynaecological Patients

NCT01412632 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 153

Last updated 2014-10-01

No results posted yet for this study

Summary

The primary endpoint is to investigate the difference in pain between patients who receive deep sedation with spontaneous breathing versus patients who receive general anesthesia.

Conditions

  • Transcervical Resection of Endometrium
  • Transcervical Resection of Fibroids
  • Transcervical Resection of Polyp

Interventions

DRUG

Remifentanil, propofol and citanest

iv remifentanil iv propofol im citanest

Sponsors & Collaborators

  • Regionshospitalet Horsens

    collaborator OTHER

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Igor Filipovski · Regionshospital Horsens

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-11-30
Primary Completion
2013-07-31
Completion
2013-08-31

Countries

  • Denmark

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 NCT01412632 on ClinicalTrials.gov