Effects of P6 stimulation on post-operative nausea and vomiting in laparoscopic cholecystectomy patients

Clinical trial comparing the P6 point stimulation and lack of stimulation in the treatment of nausea and vomiting in patients after laparoscopic cholecystectomy

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015110224799N2

Enrollment

130

Registered

2016-06-12

Start date

2005-07-23

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

postoperative nasuea and vomiting. Vomiting following gastrointestinal surgery

Interventions

Intervention 1: Intervention 1: at the point p6 under sterile conditions with disposable needles for at least 15 minutes and bran is not important. Intervention 2: Intervention 2: Not applicable.

Prevention

Intervention 1: at the point p6 under sterile conditions with disposable needles for at least 15 minutes and bran is not important

Intervention 2: Not applicable

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: Age between 18 to 80; ASA class I and II exclusion criteria: Coagulopathies; ulceration; edema; fracture at the site of stimulation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Postperative nausea. Timepoint: After awake in 1, 2 and 4 hours. Method of measurement: According to VAS scale from 0 to 10.	—

Secondary

Measure	Time frame
Vomiting after surgery. Timepoint: After awake in 1, 2 and 4 hours. Method of measurement: Severity of vomiting (mild, moderate, sever).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMajid Amini

Baqiyatallah University of Medical Sciences

amini_m1350@yahoo.com+98 21 2680 0103

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026