NCT02560064

Brief Summary

Measurement of the small bowel length studied by anatomists, surgeons and radiologists. Results were highly different among these series. Technical and mechanical factors have major effects on measures. Investigators decided to reach a standardization for the measurement of small bowel length.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
45

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2015

Shorter than P25 for all trials

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 16, 2015

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 25, 2015

Completed
1 month until next milestone

Study Start

First participant enrolled

November 1, 2015

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2016

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
Last Updated

October 5, 2015

Status Verified

September 1, 2015

Enrollment Period

2 months

First QC Date

September 16, 2015

Last Update Submit

October 2, 2015

Conditions

Small/Large Bowel

Outcome Measures

Primary Outcomes (1)

  • Length of Small Bowel. How Can Standardise Measurement and Why?

    postop 1 months

Study Arms (1)

laparotomy and small bowel length

measurement of small bowel length in laparotomies

Procedure: Laparotomy

Interventions

LaparotomyPROCEDURE

Small bowel length will measure in laparotomy, regardless of indication.

laparotomy and small bowel length

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Power analyse was done. Study include at least 44 patients.

You may qualify if:

  • Candidate for abdominal surgery

You may not qualify if:

  • Inflammatory bowel disease
  • History of intraabdominal surgery
  • peritonitis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Cerebral Palsy

Interventions

Laparotomy

Condition Hierarchy (Ancestors)

Brain Damage, ChronicBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Intervention Hierarchy (Ancestors)

Surgical Procedures, Operative

Study Officials

  • Cuneyt Kayaalp

    Inonu University, Faculty of Medicine

    STUDY DIRECTOR

Central Study Contacts

Servet Karagul

CONTACT

905334779255servetkaragul@hotmail.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
medical doctor

Study Record Dates

First Submitted

September 16, 2015

First Posted

September 25, 2015

Study Start

November 1, 2015

Primary Completion

January 1, 2016

Study Completion

February 1, 2016

Last Updated

October 5, 2015

Record last verified: 2015-09