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The Role Of Laserpuncture For Prevention Of Nausea And Vomiting Post Strabismus Surgery With General Anesthesia In Adult Patients

U

University of Indonesia (UI)

Status

Completed

Conditions

Nausea and Vomiting, Postoperative

Treatments

Device: Laserpuncture
Device: Sham Laserpuncture

Study type

Interventional

Funder types

Other

Identifiers

NCT06302673
23081229

Details and patient eligibility

About

This study to determine the effectiveness of a combination of pre-surgical laserpuncture with standard anti-emetic therapy for PONV symptoms in adult patients after strabismus surgery under general anesthesia compared to a combination of pre-surgical placebo laserpuncture with standard anti-emetic therapy. Research design using a double blinded randomized controlled trial (RCT) where research subjects and data takers who will be disguised. The research will be carried out in the Operation and Inpatient Room, Kirana Building, RSUPN Dr. Cipto Mangunkusumo (RSCM) with research subjects as adult patients undergoing strabismus surgery under general anesthesia. Assessment of nausea and vomiting using AVS ( Analog Visual Scale) consists of scoring using a score from 1-5 which indicates the severity of nausea and vomiting.

Full description

This clinical trial is to evaluate the role of laserpuncture as a prevention of nausea and vomiting in adult patients after strabismus surgery under general anesthesia. Participants are 32 males/females aged 18-59 years. They will be divided into 2 groups: (1) Group laserpuncture and (2) Sham laserpuncture. The study intervention was performed 30 minutes before surgery. The primary outcome in this study was the incidence of postoperative nausea and vomiting.

Enrollment

32 patients

Sex

All

Ages

18 to 59 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult patients aged 18-59 years.
  2. Patients undergoing simple strabismus surgery involving no more than two muscles without transposition under general anesthesia.
  3. Meets the ASA (American Society of Anesthesiologists) score of 1-2.
  4. Complete the surgical preparations according to the presedation sheet.
  5. Sign the informed consent sheet.
  6. Patients who can communicate with the research team.
  7. Patients undergoing surgery <3 hours.

Exclusion criteria

  1. The patient is pregnant.
  2. Patients who have a history of drug or drug abuse.
  3. Patients with hypersensitivity to laser light.
  4. There are wounds or skin disorders at the radiation site (skin TB, SLE(Systemic Lupus Erythematosus) skin
  5. Patients who have gastrointestinal diseases (intestinal obstruction, peristaltic disorders gastrointestinal tract, gastroenteritis, irritable bowel syndrome, dyspepsia,gastroesophageal reflux disease/GERD, appendicitis, hepatitis, cholecystitis, inflammatory bowel synchrome, pancreatitis, peptic ulcer, peritonitis, food poisoning).
  6. Patients with metabolic diseases (acid-base imbalance, metabolic diseases calcium, glucose metabolism disease, hyperlactemia, mitochondrial disease, phenylketonuria)
  7. Patients with conditions of high intracranial pressure, head trauma, migraines, disease with symptoms of seizures, vestibular diseases, malignancies, mental and psychogenic diseases, diseases arising from consumption of drugs, nephrolithiasis, other kidney diseases, myocardial infarction, as well as the occurrence of nausea and vomiting before surgery.
  8. Infection accompanied by high fever (temperature >38°C)

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

32 participants in 2 patient groups

Laserpuncture
Experimental group
Description:
Laserpuncture : using RJ Laser with Nogier B wave setting, frequency 584 Hz, power 50 mW, wavelength 785 nm, and energy of 2 Joules at each acupuncture point ( PC6 Neiguan and CV12 Zhongwan)
Treatment:
Device: Laserpuncture
Sham-Laserpuncture
Sham Comparator group
Description:
Sham Laserpuncture: The laser is turned on but not activated at each acupuncture point ( PC6 Neiguan and CV12 Zhongwan)
Treatment:
Device: Sham Laserpuncture

Trial contacts and locations

1

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Central trial contact

Yossie Faudina Putri, MD

Data sourced from clinicaltrials.gov

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