Laparoscopic Hysterectomy Clinical Trial
Official title:
Comparison of the Tissue Trauma Markers Following Total Laparoscopic Hysterectomy vs Total Abdominal Hysterectomy
Verified date | April 2020 |
Source | Mugla Sitki Koçman University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Comparison of the Tissue Trauma Markers Following Total Laparoscopic Hysterectomy vs Total Abdominal Hysterectomy
Status | Completed |
Enrollment | 40 |
Est. completion date | December 7, 2015 |
Est. primary completion date | December 7, 2015 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: ·TLH+BSO patients and TAH+BSO patients Exclusion Criteria: - History of a chronic disease (coronary artery disease, diabetes mellitus, hypertension, coronary liver failures, chronic kidney disease, chronic respiratory diseases, connective tissue disorders) which may affect levels of PTX-3 and other inflammatory markers. - Prior surgery due to malignancy. - History of an intra-abdominal surgery, except for cesarean section. - History of any disease which may lead to intra-abdominal adhesions (endometriosis, past pelvic infection). |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Mugla Sitki Koçman University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pentraxin-3 level | Pentraxin-3 ng/mL | Before 24 hours preoperatively and upto 24 hours postoperatively | |
Secondary | (NLR) | neutrophile/lymphocyte ratio | Up to 24 hours postoperative |
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