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Rib Raising for Post-operative Ileus

Randomized Controlled Trial of Rib Raising as Early Treatment for Post-operative Ileus

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03662672
Enrollment
102
Registered
2018-09-07
Start date
2018-09-27
Completion date
2019-08-30
Last updated
2022-03-10

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

Conditions

Intestinal Pseudo-Obstruction, Manipulation, Osteopathic, Osteopathic Medicine, Postoperative Care, Postoperative Complications, Postoperative Nausea and Vomiting

Brief summary

We are conducting a randomized controlled trial the use of rib raising for post-operative ileus. Rib raising is an osteopathic manipulative technique (OMT). We will recruit all patients undergoing major abdominal surgery and once they have been enrolled, we will randomize them to receive daily rib raising or a control technique where we place hands on the back but do not apply any pressure. In preliminary studies, Rib raising has been shown to reduce post-operative ileus and hospital length of stay by up to 50%.

Interventions

PROCEDURERib raising and lumbar release

Rib raising per protocol described in arm description.

PROCEDURESham procedure

Sham procedure per protocol described in arm description

Sponsors

Rutgers, The State University of New Jersey
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
No

Inclusion criteria

* Major abdominal surgery (laparotomy, laparoscopy excluding simple laparoscopic appendectomy or laparoscopic cholecystectomy)

Exclusion criteria

* Open abdomen for \>72 hours * Prior history of major post-operative complications * Intolerance to anesthesia * Co-morbidities including osteoporosis and osteopenia * Spine or rib fractures * Pregnancy * Prisoners * History of osteopathic manipulation * Recruitment delayed beyond 48 hours * Surgeon requested exclusion

Design outcomes

Primary

MeasureTime frame
Length of Stay0-14 days

Secondary

MeasureTime frame
Time to first meal0-14 days
Time to first flatus0-14 days
Time to first bowel movement0-14 days
Need for nasogastric tube postop0-14 days
Nausea/vomiting postop0-14 days

Countries

United States

Outcome results

None listed

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