Clinical trial · Interventional
Acupuncture for the Treatment of Postoperative Ileus After Gastrointestinal Surgery
A Feasibility Study of Acupuncture for the Treatment of Postoperative Ileus After Gastrointestinal Surgery
NCT04713241CI-TRIAL-00057167withdrawnN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): PI left
Summary
Brief summary (as posted)
The goal of this study is to learn if electro-acupuncture is a feasible treatment option for postoperative ileus after abdominal surgery. The second goal of this study is to evaluate the time to resolution of postoperative ileus after receiving electro-acupuncture treatments.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Gastrointestinal Cancer | Malignant Digestive System Neoplasm | ALIAS | 0.90 |
| Postoperative Ileus | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Electro-acupuncture | Procedure | — | UNRESOLVED |
| Standard of Care Bowel rest | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Group A: SOC
- description
- Participants will receive the SOC and will also be asked to complete questionnaires to rate their symptoms
- interventionNames
- Other: Standard of Care Bowel rest
- type
- EXPERIMENTAL
- label
- Group B: Electro-Acupuncture
- description
- Participants will receive the SOC + a daily 20-30 minute electro-acupuncture treatment from the time of randomization until the return of bowel function. The first treatment will be provided within 48 hours after the diagnosis of postoperative ileus. Participants will receive acupuncture every day until normal bowel movement function returns.
- interventionNames
- Procedure: Electro-acupuncture
- Other: Standard of Care Bowel rest
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 19 Years
Show eligibility criteria text
Inclusion Criteria: * Must have the ability to understand and sign a written informed consent document, and be willing to follow protocol requirements * Diagnosis of gastrointestinal cancer * Bowel resection was performed via an open or laparoscopic approach * Diagnosis of POI defined as one or more of the following criteria: 1) return to NPO status after initial attempts at oral diet, and/or 2) need for placement of nasogastric tube after surgery. * Willingness to comply with all study interventions of acupuncture Exclusion Criteria: * Active Infection at or near the acupuncture site or systemic infection (e.g. sepsis) * Physical deformities that could interfere with accurate acupuncture and point location * Concurrent use of other alternative medicines such as herbal agents and high dose vitamins and minerals * Known coagulopathy or taking heparin (including low molecular weight heparin) at full anti-coagulation doses (prophylaxis is allowed) or Coumadin at any dose. Patients on aspirin or non-steroidal anti-inflammatories or other antiplatelet medicines will be allowed to participate * Platelets \<50 H K/UL in the past 30 days * White Blood Cells (WBCs) \<3.0 K/UL or Absolute Neutrophil Count (ANC) \<1500 K/UL in the past 30 days * INR \>5 in the past 30 days * Liver failure defined as liver function test \>5x upper limit of normal * Implanted electrical device such as a cardiac pacemaker, insulin pump or pain pump * Mental incapacitation or significant emotional or psychological disorder that, in the opinion of the investigators, precludes study entry * Previous acupuncture treatment for any indications within 30 days of enrollment * Currently pregnant * Grade III lymphedema/lymphedema considered severe by the treating clinician * Chronic daily opioid use prior to admission * Enrollment in another surgical clinical trial
References
Publications (0)
Data not yet available
No reference posted for this study.