Paracetamol Absorption Technique as a Method for Measuring Gastric Tube Outlet

NCT ID: NCT02158286

Last Updated: 2014-06-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

13 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-01-31

Study Completion Date

2014-03-31

Brief Summary

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Retention of the gastric tube after esophagectomy is a clinically important problem, and there is a need of a simple method to evaluate emptying rate from the gastric tube after esophagectomy. Scintigraphy is the golden standard of measuring emptying rate from the gastric tube. In non-operated patients, paracetamol clearance technique have been widely used for measuring gastric emptying rate. There is no validation however if paracetamol clearance technique can be used for measuring emptying rate of the gastric tube. The investigators aim of this pilot- study is to validate paracetamol clearance technique to scintigraphy for measuring emptying rate from the gastric tube and to evaluate if there is a correlation between symptoms of retention and quality of life with the emptying rate.

Detailed Description

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Conditions

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Esophageal and/or Cardia Cancer Esophagectomy Gastric Pull-up Reconstruction

Study Design

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Observational Model Type

CASE_ONLY

Study Groups

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Esophagectomy, Emptying from gastric tube

Validate paracetamol clearance technique to scintigraphy for measuring emptying rate from the gastric tube.

Measuring emptying rate from the gastric tube

Intervention Type OTHER

Interventions

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Measuring emptying rate from the gastric tube

Intervention Type OTHER

Other Intervention Names

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Paracetamol clearance technique Scintigraphy

Eligibility Criteria

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Inclusion Criteria

* Patients where it had past at least two years since they had underwent an Ivor Lewis esophagectomy with gastric pull-up reconstruction.
* no signs of recurrence
* \>18 years of age

Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Region Skane

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Department of Surgery

Lund, , Sweden

Site Status

Countries

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Sweden

Other Identifiers

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TS2010

Identifier Type: -

Identifier Source: org_study_id

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