Preoperatively Walking's Effect of Postoperative Bowel Functions in Patient With Gynecologic Cancer.

• Sponsor: Bakirkoy Dr. Sadi Konuk Research and Training Hospital (Other)
• Overall Status: Completed
• CT.gov ID: NCT03553121
• Collaborator: (none)
• Enrollment: 80
• Location: 1
• Arms: 2
• Actual Duration (Months): 5.8
• Patients Per Site Per Month: 13.7

Study Details

Study Description

Brief Summary

Preoperative walking's effect of postoperative bowel functions ASA 1 or 2 in patient with gynecologic cancers.

Condition or Disease	Intervention/Treatment	Phase
Postoperative Bowel Functions	Other: walking	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 80 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Intervention Model Description: walking preoperatively not walking preoperativelywalking preoperatively not walking preoperatively
• Masking: Triple (Participant, Investigator, Outcomes Assessor)
• Masking Description: Doctor who evaluate bowel function will not know whether patients walked or not
• Primary Purpose: Prevention
• Official Title: Jinekolojik Kanserler Nedeni Ile Opere Edilen Hastalarda Preoperatif yürümenin Postoperatif Barsak fonksiyonlarına Etkisi
• Actual Study Start Date: Jan 1, 2018
• Actual Primary Completion Date: Feb 1, 2018
• Actual Study Completion Date: Jun 28, 2018

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: Walk preoperativelying Patients will be operated gynecologic cancers and have American Society of Anesthesia score 1 or 2. Subjects will walk during one hour with average speed 3 km/hour 12 hour before surgery.	Other: walking; walking and not walking
Active Comparator: not walking preoperatively Patients will be operated gynecologic cancers and have American Society of Anesthesia score 1 or 2. Subjects will not walk preoperatively.	Other: walking; walking and not walking

Outcome Measures

Primary Outcome Measures

1. the time to the first passage of flatus after surgery [6 hours- 5 days]

   Doctor will detect the time with auscultation

Secondary Outcome Measures

1. the time to first defecation [6 hours- 7 day]

   Doctor will detect the time with auscultation

2. time to first bowel movement [6 hours- 5 days]

   Doctor will detect the time with auscultation

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 80 Years
• Sexes Eligible for Study: Female
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• patients with gynecological cancer ASA score 1 or 2 via laparascopy or laparatomy

Exclusion Criteria:

• ASA score >2 orthopedic problems ileostomy or colostomy >24 hours stay in intensive care unit early postoperative complications (relaparotomy, massive blood transfusion)

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Bakirkoy Dr. Sadi Konuk Training and Research Hospital	Istanbul		Turkey	34000

Sponsors and Collaborators

• Bakirkoy Dr. Sadi Konuk Research and Training Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Bakirkoy Dr. Sadi Konuk Research and Training Hospital
• ClinicalTrials.gov Identifier: NCT03553121
• Other Study ID Numbers: 2017/223
• First Posted: Jun 12, 2018
• Last Update Posted: Jul 12, 2019
• Last Verified: Jul 1, 2019

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Bakirkoy Dr. Sadi Konuk Research and Training Hospital: gynecologic cancer; postoperative bowel function; walking; debulking

Study Results

No Results Posted as of Jul 12, 2019