Urinary Retention Clinical Trial
Official title:
Postoperative Urinary Retention and UTI After LAVH for Benign Disease
Verified date | August 2008 |
Source | Chang Gung Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Taiwan: Department of Health |
Study type | Interventional |
With the advent of minimally invasive surgery, laparoscopic assisted vaginal hysterectomy
(LAVH) is currently advocated as an alternative to abdominal hysterectomy. Reported benefits
of LAVH in short-term study, when compared with the abdominal hysterectomy, include shorter
hospital stays and convalescence, less postoperative pain, lower morbidity. To our best
knowledge, no study has been conducted to examine bladder catheterization is associated with
PUR and UTI after LAVH. No study has been performed to evaluate the long-term sequelae of
PUR after LAVH.
In this study, 150 patients undergoing LAVH are randomly assigned to have an indwelling
Foley catheter for 0 (n = 50), at 7AM-8AM in the morning of postoperative day 1 (n = 50), at
7AM-8AM in the morning of postoperative day 2 (n = 50) after the procedure by selecting a
sealed envelope, which is opened before the operation. The inclusion criteria are uterine
fibroids, endometriosis, abnormal bleeding, uterine prolapse and intra-epithelial neoplasia
of the cervix grade 3. Patients are excluded if they experienced pelvic reconstructive
surgery for pelvic organ prolapse or stress urinary incontinence; if they have bacteriuria
and clinical urinary tract symptoms, e.g. dysuria, frequency, urgency and stress
incontinence before surgery. After surgery, all patients stay at least 2 days in the
hospital. The incidences of febrile morbidity and other postoperative complications are
recorded. The outcome is assessed as immediate postoperative urinary tract symptoms, urinary
tract bacteriuria (defined as a positive culture > 105 organisms/µl), postoperative fever >
38°C and urinary retention or the inability to pass urine 6 hours after catheter remove. All
patients are followed up at 3 months and one year after surgery. To demonstrate quality of
life of women after undergo LAVH, a generic instrument of MOS Short Form 36 (SF-36) and two
specific instruments for urinary problems, Incontinence Impact Questionnaire (IIQ7) and
Urinary Distress Inventory (UDI) are asked to answer in all patients before surgery and
postoperative follow-up. All data are analyzed by the two-tailed Fisher exact test when
appropriate. Correlation coefficients are calculated to determine the associations of
preoperative, intraoperative, and postoperative factors with the incidence of postoperative
urinary retention and positive urine cultures. A value of p < 0.05 is considered
statistically significant.
Status | Completed |
Enrollment | 150 |
Est. completion date | July 2008 |
Est. primary completion date | January 2008 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 34 Years to 68 Years |
Eligibility |
Inclusion Criteria: - Uterine fibroids - Endometriosis - Abnormal bleeding - Uterine prolapse and intra-epithelial neoplasia of the cervix grade 3 Exclusion Criteria: - If they experienced pelvic reconstructive surgery for pelvic organ prolapse or stress urinary incontinence - If they have bacteriuria and clinical urinary tract symptoms, e.g. dysuria, frequency, urgency and stress incontinence before surgery |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Chang Gung Memorial Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | all cause mortality | one year | Yes |
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