Idiopathic Thrombocytopenic Purpura Clinical Trial
Official title:
Single Incision Versus Standard Laparoscopic Splenectomy
Verified date | February 2017 |
Source | Children's Mercy Hospital Kansas City |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a prospective trial of single incision versus standard 4-port laparoscopic
splenectomy.
The hypothesis is that there may be a difference in wound infection rates, operative time,
doses of analgesics post-operatively, and patient/parent perception of scars. However, the
technical difficulty is considerable and the primary outcome is operative time which will be
expressed in minutes.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | April 2017 |
Est. primary completion date | October 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 1 Year to 18 Years |
Eligibility |
Inclusion Criteria: - Need for splenectomy Exclusion Criteria: - Splenomegaly |
Country | Name | City | State |
---|---|---|---|
United States | Children's Mercy Hospital | Kansas City | Missouri |
Lead Sponsor | Collaborator |
---|---|
Children's Mercy Hospital Kansas City |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Operative time | operative time | 1 day | |
Secondary | operative complications | 1 day | ||
Secondary | wound complications | 1 month | ||
Secondary | cosmesis | 6 months | ||
Secondary | length of stay | 1 week | ||
Secondary | operative difficulty | 1 day |
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