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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00674713
Other study ID # 1014/05
Secondary ID
Status Completed
Phase Phase 4
First received May 5, 2008
Last updated May 7, 2008
Start date January 2006
Est. completion date September 2007

Study information

Verified date May 2008
Source Catholic University of the Sacred Heart
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

The aim of the study is to investigate if P6 acupuncture made after induction of general anaesthesia might be effective for the prevention of PONV as ondansetron and if the acupuncture-ondansetron combination could enhance single therapy efficacy in patients undergoing laparoscopic cholecystectomy.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date September 2007
Est. primary completion date September 2007
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients ASA I-II scheduled for elective laparoscopic cholecystectomy.

Exclusion Criteria:

- Patient's refusal

- Patients with history of carpal tunnel syndrome or eczema at P6 point

- Pregnant patients

- Female patients in a phase of the menstrual cycle other than premenstrual, nausea and vomiting within 24 hours before anaesthesia

- Known allergy to anti-inflammatory drugs, opioids and ondansetron.

- Patients with a pre-existing chronic pain disorder or with a gastrointestinal disease.

Study Design

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


Related Conditions & MeSH terms


Intervention

Other:
Acupuncture

Drug:
Ondansetron

Physiological saline solution

Other:
Sham acupuncture

Drug:
Ondansetron

Other:
Acupuncture at P6 point

Drug:
Physiological saline solution

Other:
Sham acupuncture


Locations

Country Name City State
Italy Catholic University of Sacred Heart Rome

Sponsors (1)

Lead Sponsor Collaborator
Catholic University of the Sacred Heart

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative nausea and vomiting 24 postoperative hours No
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