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Treatment of Functional Dyspepsia With Acupuncture

Treatment of Functional Dyspepsia With Acupuncture: A Randomized, Blinded, Sham Acupuncture Controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00786214
Enrollment
42
Registered
2008-11-06
Start date
2007-02-28
Completion date
2009-12-31
Last updated
2013-06-21

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

Conditions

Functional Dyspepsia

Keywords

Functional Dyspepsia, Acupuncture, Traditional Chinese Medicine

Brief summary

Functional dyspepsia (FD) is one of the most common chronic gastrointestinal disorders affecting humans. Existing therapies for FD are still far from satisfactory and new therapies are constantly being sought. Acupuncture has been used for the alleviation of functional gastrointestinal symptoms in several non-controlled studies. This study aims to investigate the therapeutic efficacy of acupuncture in patients with FD.

Interventions

OTHERAcupuncture

Patients will be stimulated at specific acupuncture points as determined for treatment of the disease by certified acupuncturists

OTHERSham acupuncture

Patients will be given sham acupuncture treatment at dummy acupuncture points

Sponsors

National University Hospital, Singapore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

\- female and male patients with functional dyspepsia between the ages of ≥18 and ≤70 years. FD will be diagnosed according to the Rome-III criteria. Onset of FD symptoms should begin at least 6 months before clinical presentation and must be fulfilled for the last 3 months and his or her FD symptoms score must be of at least moderate severity.

Exclusion criteria

* Subjects unable to give informed consent * Pregnant or breast-feeding females or women who get pregnant midway * Subjects who have received acupuncture treatment before * Subjects who have had a previous gastrointestinal surgery except appendectomy and laparoscopic cholecystectomy * Any significant past or concurrent disease or disorder which, in the opinion of the investigator, may either put subject at risk in the study, influence the results of the study or influence subject's ability to participate in the study * Maintenance treatment with PPIs (proton pump inhibitors) and H2RAs (H2-receptor antagonists) continuously (every day) in the last 6 months prior to entry into the study * Treatment with PPIs and H2RAs, prokinetics, antibiotics, prostaglandins or bismuth-containing compounds during the last 2 weeks prior to entry into the study * H. pylori eradication treatment within the past 12 months before study start * H. pylori positive patients * Patients with bleeding diathesis * Known or suspected hypersensitivity to acupuncture.

Design outcomes

Primary

MeasureTime frame
Resolution of symptoms4 weeks

Secondary

MeasureTime frame
Health-related quality of life and hospital anxiety & depression scale4 weeks

Countries

Singapore

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026