Differences in Peritoneal Stem Cells in Women With and Without Adhesions After Gynaecological Surgery
NCT ID: NCT02847676
Last Updated: 2016-07-28
Study Results
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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UNKNOWN
40 participants
OBSERVATIONAL
2016-08-31
2017-08-31
Brief Summary
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Detailed Description
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After all surgeries cytokine induced fibrotic bands appear within 72 hours. Usually those bands are eliminated by a fibrinolytic sequence within 10 days.
For Adhesions that persist afterwards the generally accepted assumption is, that there is a failure of the fibrinolytic sequence with unknown origin. Adhesions which persist for more than 10-14 days become thicker and vascularised. In those "adult" adhesions not only fibrin is found but also fat tissue, smooth muscles and myelinised and un - myelinised axons.
In developmental biology those tissues differentiate from different germ layers, namely mesoderm and ectoderm. Finding cells from multiple germ layers points towards a pluri -, multi-, or stem cell like precursor cell from which those adhesions develop. Such a cellpopulation has not been characterised in the abdomen to the date of writing, though Studies have shown evidence (ranging from mesothelial - to - mesenchymal shift to Clusters of differentiation from multiple germ layers) which made multiple researchers postulate a pluripotent precursor cell located in the submesothelium.
In our research we will therefore take peritoneal samples from adhesions, peritoneal wall lining and omentum in subjects with and without peritoneal adhesions in subjects undergoing indicated laparoscopic surgery at the gynaecological ward at the Pius hospital in Oldenburg.
The samples are routinely taken as part of the procedure and usually discarded. At least 24 hours prior to surgery, the subjects will have a chance to give their informed consent to donate those samples for our study. The study is thus designed in a way that subjects won't undergo additional risk by participating in the study. Taking part or the refusal hereof won't have any effect on the treatment or surgical outcome for the subjects. Also, taking part in our study won't have any benefits or additional risks for the subjects.
The samples will then be taken to the university of Leipzig, where we will culture, isolate and characterise the cells. Characterisation will mostly be the application of pluripotency markers, cell sorting and immunoassays. Expression profiles will be used to further understand the mesothelial - to - mesenchymal shift. Depending on our findings the protocol for analysis will be adjusted in consultation with Prof. dr. dr. De Wilde and Prof. dr. Bader.
The study will approximately take 6 months, with an additional 6 months for writing and publication. The study is funded by the research funding pool of the university of Oldenburg.
Conditions
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Study Groups
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No previous surgery, adhesions present.
Patients have had no previous abdominal surgery. Inspection shows peritoneal adhesions.
Tissue sample donation
Patients undergo planned gynaecological surgery. Tissue samples, which are routinely taken, are donated.
No previous surgery, no adhesions present.
Patients have had no previous abdominal surgery. Inspection shows no peritoneal adhesions.
Tissue sample donation
Patients undergo planned gynaecological surgery. Tissue samples, which are routinely taken, are donated.
Previous surgery, adhesions present.
Patients have had previous abdominal surgery. Inspection shows peritoneal adhesions.
Tissue sample donation
Patients undergo planned gynaecological surgery. Tissue samples, which are routinely taken, are donated.
Previous surgery, no adhesions present.
Patients have had previous abdominal surgery. Inspection shows no peritoneal adhesions.
Tissue sample donation
Patients undergo planned gynaecological surgery. Tissue samples, which are routinely taken, are donated.
Interventions
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Tissue sample donation
Patients undergo planned gynaecological surgery. Tissue samples, which are routinely taken, are donated.
Eligibility Criteria
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Inclusion Criteria
2. Woman with a negative pregnancy test at the time of recruitment, and sufficient contraception from time of
3. Woman with any gynecological pathology requiring scheduled pelvic gynecological surgery, either laparotomy or laparoscopy.
4. Woman without primary peritoneal disease.
Exclusion Criteria
2. Emergency surgery
3. Patients under systemic immunosuppressive therapy in the previous 6 months
4. Patients with current intra-abdominal or pelvic abscess or systemic infection
5. Pregnant woman
6. Simultaneous participation in another clinical trail
18 Years
FEMALE
Yes
Sponsors
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University of Leipzig
OTHER
University of Oldenburg
OTHER
Pius-Hospital Oldenburg
OTHER
Responsible Party
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Prof. Dr. Dr. med. Rudy Leon De Wilde
Prof. Dr. Dr. med
Central Contacts
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Other Identifiers
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PHDW-005
Identifier Type: -
Identifier Source: org_study_id
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