Standard Carbon Dioxide Gas Versus Heated Humidified Gas in Gynaecological Laparoscopy
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|ClinicalTrials.gov Identifier: NCT02319902|
Recruitment Status : Unknown
Verified December 2014 by Fevzi Shakir, Royal Surrey County Hospital NHS Foundation Trust.
Recruitment status was: Recruiting
First Posted : December 18, 2014
Last Update Posted : December 18, 2014
|Condition or disease||Intervention/treatment||Phase|
|Heated Humidified Carbon Dioxide in Gynaecological Laparoscopic Surgery||Device: Standard cold carbon dioxide gas Device: Heated humidified carbon dioxide gas||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||88 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Double (Participant, Outcomes Assessor)|
|Official Title:||The Effects of Using Heated Humidified Carbon Dioxide Gas on Post Operative Pain Scores, Nausea and Analgesic Requirements in Patients Undergoing Gynaecological Laparoscopy: a Randomised Controlled Trial.|
|Study Start Date :||December 2014|
|Estimated Primary Completion Date :||December 2015|
|Estimated Study Completion Date :||December 2015|
Placebo Comparator: Standard cold carbon dioxide gas
Standard cold carbon dioxide gas
Device: Standard cold carbon dioxide gas
Use of standard cold carbon dioxide gas in laparoscopic gynaecological surgery.
Active Comparator: Heated humidified carbon dioxide gas
Heated humidified carbon dioxide gas
Device: Heated humidified carbon dioxide gas
Use of the Fischer and Paykel heated humidification system for laparoscopic gynaecological surgery.
- Shoulder tip pain [ Time Frame: 8 hours ]Shoulder tip pain recorded as a visual analogue scale from 1-10, 8 hours post surgery compared to baseline
- General abdominal pain, nausea, vomiting and analgesia requirements [ Time Frame: 8 hours ]General abdominal pain, nausea, vomiting and analgesia requirements 8 hours post surgery compared to baseline
- Shoulder tip pain, general abdominal pain, nausea, vomiting. [ Time Frame: 7 days ]Shoulder tip pain, general abdominal pain, nausea, vomiting over a 7 day period compared to baseline
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02319902
|Contact: Fevzi Shakir, MBBS BSc MRCOGemail@example.com|
|Contact: Andrew Kent, TD MD FRCOGfirstname.lastname@example.org|