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Study About Effect of Preoperative Bowel Preparation Versus no Bowel Preparation Before Spinal Surgery

Preoperative Bowel Preparation Versus no Preparation Before Spinal Surgery: a Randomised Clinical Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01879605
Enrollment
45
Registered
2013-06-18
Start date
2007-12-31
Completion date
2009-12-31
Last updated
2013-06-18

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

Conditions

Constipation, Ileus, Surgery

Keywords

Spinal surgery, Bowel preparation, Ileus, Constipation, Well-being

Brief summary

This study investigated the effect of preoperative bowel preparations for patients undergoing spinal fusion surgery.

Detailed description

This was a randomised clinical trial with one control group and two treatment groups. Forty-five elective spinal fusion patients were randomised into three groups who received preoperative treatment with either enema of sorbitol and docusat natrium, Bisacodyl suppository or no bowel preparation.

Interventions

DRUGDocusate natrium and sorbitol
DRUGBisacodyl

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients undergoing spinal fusion surgery * Age 15 years or older * The patients had to understand oral and written Norwegian. * Postoperative pain management via epidural catheter should have been planned. *

Exclusion criteria

* Constipation * Regularly use of enema

Design outcomes

Primary

MeasureTime frame
Defecation within 72 hours postoperativelyThe study's outcome measures were recorded every evening between 17.00 and 21.00 hours

Secondary

MeasureTime frame
Postoperative constipationThe study's outcome measures were recorded every evening between 17.00 and 21.00 hours

Other

MeasureTime frame
The study's outcome measures were recorded every evening between 17.00 and 21.00 hoursNausea
PainThe study's outcome measures were recorded every evening between 17.00 and 21.00 hours

Countries

Norway

Outcome results

None listed

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