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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT02086461
Other study ID # 2013/896-31/4
Secondary ID 2013/896-31/4
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date December 2020

Study information

Verified date January 2019
Source Karolinska University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Delayed emptying of the gastric tube after esophagectomy is a frequent and durable problem. No treatment is currently available. It can be hypothesized that incomplete relaxation of the pyloric sphincter may be a significant contributing factor. Pneumatic dilatation may therefore be a potentially effective treatment.


Description:

Patients surviving one year after esophagectomy are sent questionnaires to pick up symptoms suggestive of delayed gastric emptying.Those fulfilling predefined criteria for delayed gastric emptying will be invited to the study. The study design is sham controlled single blind with a follow up extending to twelve months post treatment.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date December 2020
Est. primary completion date December 2020
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Previous esophagectomy and gastric tube reconstruction.

- Symptoms suggestive of delayed gastric emptying.

- signed informed consent

Exclusion Criteria:

- Signs of recurrent cancer disease

- no symptoms suggestive of delayed gastric emptying.

- unwillingness to participate

Study Design


Intervention

Device:
Pneumatic pyloric dilatation

Other:
15 mm pyloric balloon dilatation


Locations

Country Name City State
Sweden Karolinska University Hospital Stockholm

Sponsors (6)

Lead Sponsor Collaborator
Karolinska University Hospital Lund University Hospital, Region Örebro County, Sahlgrenska University Hospital, Sweden, University Hospital, Linkoeping, Uppsala University Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Symptoms suggestive of delayed gastric emptying Symptoms will be assessed at 3, 6 and 12 months after therapy. In case of failure the code will be broken and if sham procedure has been done the patient will be offered pneumatic dilatation. 3-12 months after treatment
Secondary Quality of Life Symptoms will be assessed at 3, 6 and 12 months after therapy. In case of failure the code will be broken and if sham procedure has been done the patient will be offered pneumatic dilatation. 3-12 months after treatment.
Secondary Delayed gastric emptying Symptoms will be assessed at 3, 6 and 12 months after therapy. In case of failure the code will be broken and if sham procedure has been done the patient will be offered pneumatic dilatation. Paracetamol test done only 3 months after treatment. 3, 6 and 12 months after treatment.
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