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Effectiveness of auricular acupressure for prevention of postoperative nausea and vomiting in adult patients undergoing major abdominal surgeries without large incisions on skin.

Effectiveness of auricular acupressure for prevention of postoperative nausea and vomiting in adult patients undergoing elective abdominal laparoscopic surgeries under general anaesthesia, a prospective controlled study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044284
Enrollment
120
Registered
2022-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

None listed

Interventions

Intervention1: AURICULAR ACUPRESSURE FOR PONV: All group I patients( case group receiving auricular acupressure) will also receive IV ramosetron and IV dexamethasone as a part of premedication duri

Sponsors

JSS AHER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i)Adults of ASA physical status I/II ii)age - 18 to 60 years iii) surgical procedure - elective abdominal laparoscopic surgeries ( laproscopic cholecystectomy , laproscopic appendicectomy , total laproscopic hysterectomy) iv)Surgical duration less than 3 hours

Exclusion criteria

Exclusion criteria: Patients already on treatment with anti-emetics, steroid medication, or any other drug known to cause emesis currently or in the immediate past , Auricular pain , Allergy to adhesive tape, Hypersensitivity reaction to Ramosetron or Dexamethasone , Pregnant or nursing mothers , Vomiting within 24 hours before surgery or of any organic etiology.

Design outcomes

Primary

MeasureTime frame
To know the efficacy of triple therapy: Auricular acupressure, IV ramosetron 0.3mg & dexamethasone 4mg in prevention of PONV in adult patients undergoing elective abdominal laparoscopic surgeries under general anaesthesia, by the end of 24 hours from the beginning of surgery.Timepoint: Every 2nd hourly during intra-operative period and after 6 hours and 24hrs of post surgery.

Secondary

MeasureTime frame
TO ASSESS : Severity of PONV , Number of rescue antiemetic medications required , Assessment of Aphel scoring and comparison with the incidence and severity of PONV, by the end of 24 hours post-surgery.Timepoint: Every second hourly during intra operative period and and after 6 hours and 24 hours during post operative period.

Countries

India

Contacts

Public ContactDr Harish Kumar P

JSS Academy of Higher Education and Research, Deemed to be University

harishkumarp@jssuni.edu.in9686527230

Outcome results

None listed

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