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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02943525
Other study ID # PACKING
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 14, 2016
Est. completion date December 2024

Study information

Verified date August 2023
Source Charles University, Czech Republic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Vaginal packing is used routinely following vaginal reconstructive surgery, however, no recommendation regarding vaginal packing after laparoscopic sacrocolpopexy exists. Despite little data to support the practice, purported benefits better positioning and fixation of the mesh, improving incorporation of the mesh by its fixation and reduced blood loss. Patients often complain of discomfort associated with the packing or its removal. The aim of this randomized controlled is to compare the subjective impressions of pain and bother in women undergoing laparoscopic sacrocolpopexy treated with and without packing. The investigators also aim to assess differences in postoperative bacteriuria, urine retention and hemoglobin levels on day 5 after the surgery and surgery outcome and complications at one year after the surgery in those with and without packing.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 253
Est. completion date December 2024
Est. primary completion date June 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - Laparoscopic sacrocolpopexy without a suburethral sling - Pelvic organ prolapse stage > 2 - Speak and read Czech - Can to understand the informed consent Exclusion Criteria: - Any other surgery than sacrocolpopexy - Concurrent hysterectomy or opening of the vagina during the surgery. - Vaginal, uterine, cervical or ovarian malignancy - Clotting disorder, taking anticoagulation - Having intraoperative blood loss greater than 500 ml

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
vaginal packing
Packing vagina with a Boric acid soaked gauze at the end of surgery

Locations

Country Name City State
Czechia Department of Obstetrics and Gynecology, Charles University Hospital Pilsen

Sponsors (1)

Lead Sponsor Collaborator
Charles University, Czech Republic

Country where clinical trial is conducted

Czechia, 

References & Publications (2)

Thiagamoorthy G, Khalil A, Cardozo L, Srikrishna S, Leslie G, Robinson D. The value of vaginal packing in pelvic floor surgery: a randomised double-blind study. Int Urogynecol J. 2014 May;25(5):585-91. doi: 10.1007/s00192-013-2264-y. Epub 2013 Dec 6. — View Citation

Westermann LB, Crisp CC, Oakley SH, Mazloomdoost D, Kleeman SD, Benbouajili JM, Ghodsi V, Pauls RN. To Pack or Not to Pack? A Randomized Trial of Vaginal Packing After Vaginal Reconstructive Surgery. Female Pelvic Med Reconstr Surg. 2016 Mar-Apr;22(2):111-7. doi: 10.1097/SPV.0000000000000238. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative pain assessed using VAS Visual analog scale (VAS) The first post-operative day before extraction of the packing
Primary Satisfaction with the overall postoperative course assessed using VAS VAS Postoperative day 5
Primary Prolapse recurrence Pelvic Organ Prolapse Quantification System (POP-Q) classification - the most descending compartment >-1cm from hymen 1 year after the surgery
Primary Surgery related complications According to the International Continence Society / International UroGynecology Association Joint Terminology and Classification Report of the complications related directly to the insertion of prostheses (meshes, implants, tapes) & grafts in female pelvic floor surgery From the surgery until 1 year after the surgery
Primary Postoperative pain assessed using the McGill Questionnaire McGill Questionnaire The first post-operative day before extraction of the packing
Secondary Number of analgesics used From the end of the surgery until the first postoperative day
Secondary Positive urine culture Postoperative day 5
Secondary Satisfaction with surgery assessed using VAS VAS Postoperative day 1 before packing extraction
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