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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01442961 |
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Date of registration:
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19/09/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Vaginal Hysterectomy, Laparoscopic Hysterectomy, Postoperative Pain
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Scientific title:
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Postoperative Pain After Vaginal or Laparoscopic Hysterectomy: a Prospective Trial |
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Date of first enrolment:
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January 2009 |
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Target sample size:
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188 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01442961 |
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Study type:
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Interventional |
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Study design:
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Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Finland
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Age 18 -69 years
- Gender . female
- ASA status 1-3
- Vaginal hysterectomy or laparoscopic hysterectomy
Exclusion Criteria:
- Body mass Index over 35
- Diabetes Mellitus
- Liver disease
- Allergies to pharmaceuticals used in the Study
- Present use of opioids
- Vaginal prolapse
Age minimum:
18 Years
Age maximum:
69 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Postoperative Pain
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Intervention(s)
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Procedure: laparoscopy, laparoscopic hysterectomy
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Procedure: vaginal : vaginal hysterectomy
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Primary Outcome(s)
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Postoperative consumption of an opioid (oxycodone)
[Time Frame: 20 hours]
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Secondary Outcome(s)
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NRS (numeral rating scale) of pain
[Time Frame: 20 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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