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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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12 December 2020 |
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Main ID: |
NCT03159637 |
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Date of registration:
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17/05/2017 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Pneumoperitoneum and Gynecological Laparoscopic Surgery: An Observational Clinical Study
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Scientific title:
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Impact Of Posture and Prolonged Pneumoperitoneum on Intra-Operative and Postoperative Outcomes During Gynecological Laparoscopic Surgery: An Observational Clinical Study |
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Date of first enrolment:
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May 30, 2017 |
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Target sample size:
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60 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03159637 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Egypt
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Contacts
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Name:
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Sayed K Abd-Elshafy, M.D |
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Address:
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Telephone:
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Email:
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Affiliation:
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Associate Profossor |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
1. Age range 18-50
2. ASA 1
3. Elective gynecological laparoscopic surgery
Exclusion Criteria:
1. Severe ischemic or valvular heart disease
2. Increased intracranial pressure (e.g. Hydrocephalus, Cerebral tumor, Head injury)
3. Hepatic or renal impairment
4. Emergency surgery
5. Open surgery
6. Previous abdominal surgery
Age minimum:
18 Years
Age maximum:
50 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Laparoscopy
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Intervention(s)
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Procedure: Laparoscopic Surgery
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Primary Outcome(s)
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mean arterial blood pressure
[Time Frame: within the duration of the operation]
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Pulmonary function tests
[Time Frame: within the first 24 hours]
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Secondary Outcome(s)
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Analgesic requirement
[Time Frame: within the first 24 hours]
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Intra-abdominal pressure
[Time Frame: within the first 24 hours]
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PaO2
[Time Frame: within the first 24 hours]
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Arterial to end-tidal PaCO2- difference
[Time Frame: within the first 24 hours]
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Postoperative nausea and vomiting
[Time Frame: within the first 24 hours]
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Secondary ID(s)
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IRB000087698
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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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