Skip to content

Effect of Laser Acupuncture on Adhesive Small Bowel Obstruction

Effect of Laser Acupuncture on Adhesive Small Bowel Obstruction: a Prospective Double-blind Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04318821
Enrollment
30
Registered
2020-03-24
Start date
2020-03-01
Completion date
2023-02-28
Last updated
2026-08-17

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

Conditions

Adhesive Small Bowel Obstruction

Keywords

Adhesive small bowel obstruction, Laser acupuncture, Acupuncture

Brief summary

Adhesive small bowel obstruction (ASBO) is one of the most common complications and is a major cause of admission after intra-abdominal surgery. To date, the ideal management of ASBO remains controversial. The aim of this protocol designed as a double-blind randomized controlled trial is to investigate the efficacy of laser acupuncture (LA) therapy in patients with ASBO.

Interventions

PROCEDURELaser acupuncture

Laser acupuncture is a non-invasive therapy that involves stimulation of traditional acupoints with low-intensity, non-thermal laser irradiation.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

The participants in each group will receive real (with energy output) or sham (without energy output) laser acupuncture. The feelings of participants in each group are not different. The care provider and outcomes assessor don't involve the random allocation and don't know if participants receive real laser acupuncture.

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Aged 20 to 80 years * Clinical symptoms and signs of mechanical obstruction

Exclusion criteria

* Clear non-adhesive etiology of small bowel obstruction (e.g. tumor, hernia) * Emergency surgical intervention before being admitted to the hospital * Pregnancy * Local skin infection on the acupoints, and limb amputees.

Design outcomes

Primary

MeasureTime frameDescription
Success rate of conservative treatment2 weekDefined as no need for long term nasogastric tube decompression and operative intervention.

Secondary

MeasureTime frameDescription
Time to oral intake2 weeksDefined as participants can try intake due to symptoms improved including nausea, vomiting, distension and pain.
Length of hospital stayThrough study completion, an average of 1 yearDate from admission to discharge
Serum lipaseUp to 2 weeksSerum lipase
Serum amylaseUp to 2 weeksSerum amylase
Serum cortisolUp to 2 weeksSerum cortisol
Serum motilinUp to 2 weeksSerum motilin
Serum ghrelinUp to 2 weeksSerum ghrelin
Serum intestinal fatty acid binding protein (I-FABP)Up to 2 weeksSerum intestinal fatty acid binding protein (I-FABP)

Countries

Taiwan

Contacts

PRINCIPAL_INVESTIGATORChun-Ting Liu, MD

Department of Chinese Medicine, Kaohsiung Chang Gung Memorial Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026