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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02319902
Other study ID # 14SURN0015
Secondary ID
Status Recruiting
Phase N/A
First received December 14, 2014
Last updated December 14, 2014
Start date December 2014
Est. completion date December 2015

Study information

Verified date December 2014
Source Royal Surrey County Hospital
Contact Fevzi Shakir, MBBS BSc MRCOG
Email fevzi@doctors.org.uk
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

To establish if heated humidified carbon dioxide gas improves pain scores as well as nausea and analgesic requirements in post operative patients compared to standard cold carbon dioxide.


Recruitment information / eligibility

Status Recruiting
Enrollment 88
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients over 18 years of age

- Patients planned to undergo laparoscopy for minor procedures such as endometriosis, adhesions, ovarian cystectomies, bilateral salpingoophorectomy, tubal ligation and sterilisation will be invited to participate in the trial.

- Capacity to consent

Exclusion Criteria:

- Patients unable to speak English

- Patients unable to give consent

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Heated Humidified Carbon Dioxide in Gynaecological Laparoscopic Surgery

Intervention

Device:
Standard cold carbon dioxide gas
Use of standard cold carbon dioxide gas in laparoscopic gynaecological surgery.
Heated humidified carbon dioxide gas
Use of the Fischer and Paykel heated humidification system for laparoscopic gynaecological surgery.

Locations

Country Name City State
United Kingdom Royal Surrey County Hospital NHS Trust Guildford Surrey

Sponsors (1)

Lead Sponsor Collaborator
Fevzi Shakir

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Shoulder tip pain Shoulder tip pain recorded as a visual analogue scale from 1-10, 8 hours post surgery compared to baseline 8 hours No
Secondary General abdominal pain, nausea, vomiting and analgesia requirements General abdominal pain, nausea, vomiting and analgesia requirements 8 hours post surgery compared to baseline 8 hours No
Secondary Shoulder tip pain, general abdominal pain, nausea, vomiting. Shoulder tip pain, general abdominal pain, nausea, vomiting over a 7 day period compared to baseline 7 days No