ClinicalTrials.Veeva

Menu

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

University of Oslo (UIO) logo

University of Oslo (UIO)

Status and phase

Completed
Phase 4

Conditions

Ileus
Surgery
Constipation

Treatments

Drug: Bisacodyl
Drug: Docusate natrium and sorbitol

Study type

Interventional

Funder types

Other

Identifiers

NCT01879605
v57e4nbn

Details and patient eligibility

About

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

Full 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.

Enrollment

45 patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Enema
Experimental group
Description:
Docusate natrium and sorbitol, 240 ml enema, the evening before surgery
Treatment:
Drug: Docusate natrium and sorbitol
Suppository
Active Comparator group
Description:
Bisacodyl, suppository 10 mg, the evening before surgery.
Treatment:
Drug: Bisacodyl
Control grup
No Intervention group
Description:
No intervention

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems