Closure of Vaginal Cuff at Laparoscopic Hysterectomy
Conditions
Brief summary
This study compares outcomes among patients having a total laparoscopic hysterectomy. This involves removing the uterus and cervix using a laparoscopic or keyhole technique. The top of the vagina is routinely sutured closed after this procedure and this study is comparing two different suture materials for this purpose. One suture material is a barbed suture that has the advantage of maintaining good tension and closure on the wound. The other is a standard smooth suture that is commonly used for this procedure. The investigators are comparing the time it takes to close the vaginal cuff, as well as bleeding after surgery and the healing of the top of the vagina.
Detailed description
Barbed suture has been used to close the vaginal vault for almost 3 years now, and a few preliminary studies report positive outcomes. Unfortunately, the retrospective nature of these studies may present outcomes in an overly positive light, since some of the patients may not be able to remember all the potential complications or problems they may have had in the immediate postoperative period (recall bias). The current standard of care for vaginal cuff closure appears to be to use Vicryl suture although practices vary widely. The specific aim of this study is to evaluate whether the use of barbed suture facilitates the laparoscopic closure of the vaginal cuff during a total laparoscopic hysterectomy. The inclusion criteria for our study include all patients who are planned for a total laparoscopic hysterectomy due to benign conditions such as symptomatic uterine fibroids, abnormal uterine bleeding, endometriosis and pelvic pain. The laparoscopic hysterectomy will proceed as per routine. For vaginal cuff closure with barbed suture we will use a 0 polydioxanone (PDO) bidirectional barbed suture on a 36 mm half-circle taper point needle. For cuff closure with Vicryl, we plan to use 2/0 Vicryl with the vaginal cuff closure proceeding in a similar fashion as with the barbed suture. Regardless of suture material used it is important to obtain a full thickness bite with a 1 cm margin on the vagina mucosa on each bite. Patients will be stratified to either closure by the attending or the resident or fellow under the supervision of the attending. The resident or fellow will have 15 minutes to complete the vaginal cuff closure. If they are not able to complete it within that time frame, the attending will take over and complete the vaginal cuff closure. This is to avoid adding excess operating time to the procedure due to having a trainee performing a portion of the procedure. Patients will also be asked to complete a short survey regarding dyspareunia as well as a standardized sexual function questionnaire (FSFI) prior to surgery and 3 months after surgery to evaluate if the use of barbed suture affects this in any way. Further we will also inquire about male dyspareunia before and after surgery for the same reason. Patients will be examined at a postoperative visit 3 weeks after surgery and vaginal cuff granulation and any evidence of vaginal cuff infection or separation will be carefully examined and documented. Patients will be called 3 months after surgery to inquire about any dyspareunia, male dyspareunia, vaginal bleeding or readmissions to the hospital. We are interested in evaluating dyspareunia, since a concern has been raised that the use of barbed suture at the vaginal apex may result in dyspareunia and partner dyspareunia. Although we have not found this to be the case in our clinical experience we would like to evaluate this point, especially since the use of barbed suture for closing the vaginal cuff has become a common practice nationwide. Patients will be dismissed from the trial after the 3 month follow up.
Interventions
Closure of the vaginal cuff
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients having a total laparoscopic hysterectomy for benign conditions
Exclusion criteria
* Malignancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Vaginal Cuff Closure Time | During the surgical procedure | Average time (measured in minutes) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Dyspareunia | Postoperative | Assessed preoperatively and up to 3 months postop |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Barbed Vaginal cuff closure with barbed suture
Closure of vaginal cuff: Closure of the vaginal cuff | 32 |
| Smooth Vaginal cuff closure with smooth suture
Closure of vaginal cuff: Closure of the vaginal cuff | 31 |
| Total | 63 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Withdrawal by Subject | 0 | 1 |
Baseline characteristics
| Characteristic | Smooth | Total | Barbed |
|---|---|---|---|
| Age, Continuous | 43.2 years STANDARD_DEVIATION 8.1 | 44.7 years STANDARD_DEVIATION 0.71 | 46.1 years STANDARD_DEVIATION 5.6 |
| BMI | 26.9 kg/m^2 STANDARD_DEVIATION 8.6 | 28.0 kg/m^2 STANDARD_DEVIATION 4.2 | 29.1 kg/m^2 STANDARD_DEVIATION 5.9 |
| Cuff closure performed by the Attending Surgeon or the Fellow/Resident Attending | 15 participants | 31 participants | 16 participants |
| Cuff closure performed by the Attending Surgeon or the Fellow/Resident Fellow/Resident | 16 participants | 32 participants | 16 participants |
| Gender Female | 31 Participants | 63 Participants | 32 Participants |
| Gender Male | 0 Participants | 0 Participants | 0 Participants |
| Hospital Army Hospital | 13 participants | 27 participants | 14 participants |
| Hospital Brigham and Women's Hospital | 11 participants | 22 participants | 11 participants |
| Hospital Faulkner Hospital | 7 participants | 14 participants | 7 participants |
| Marital Status - Married | 12 participants | 23 participants | 11 participants |
| Medical History Abnormal Uterine Bleeding | 24 participants | 51 participants | 27 participants |
| Medical History Fibroids | 20 participants | 41 participants | 21 participants |
| Medical History Infertility | 2 participants | 5 participants | 3 participants |
| Medical History Pelvic Pain | 24 participants | 47 participants | 23 participants |
| Medical History Prior Laparoscopy | 12 participants | 27 participants | 15 participants |
| Medical History Prior Laparotomy | 19 participants | 31 participants | 12 participants |
| Medical History Prolapse | 0 participants | 0 participants | 0 participants |
| Parity | 1.7 Births STANDARD_DEVIATION 1 | 1.7 Births STANDARD_DEVIATION 0 | 1.7 Births STANDARD_DEVIATION 1.3 |
| Race/Ethnicity, Customized Asian | 1 participants | 3 participants | 2 participants |
| Race/Ethnicity, Customized Black | 8 participants | 16 participants | 8 participants |
| Race/Ethnicity, Customized Hispanic | 2 participants | 4 participants | 2 participants |
| Race/Ethnicity, Customized Other | 1 participants | 1 participants | 0 participants |
| Race/Ethnicity, Customized Unknown | 0 participants | 1 participants | 1 participants |
| Race/Ethnicity, Customized White | 19 participants | 38 participants | 19 participants |
| Region of Enrollment United States | 31 participants | 63 participants | 32 participants |
| Sexual Function Any female dyspareunia reported | 13 participants | 25 participants | 12 participants |
| Sexual Function Any male dyspareunia reported | 0 participants | 0 participants | 0 participants |
| Sexual Function Ongoing problem | 0 participants | 5 participants | 5 participants |
| Sexual Function Other | 0 participants | 0 participants | 0 participants |
| Smoking Status - Smoker | 7 participants | 9 participants | 2 participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — |
| other Total, other adverse events | 0 / 32 | 0 / 31 |
| serious Total, serious adverse events | 0 / 32 | 0 / 31 |
Outcome results
Vaginal Cuff Closure Time
Average time (measured in minutes)
Time frame: During the surgical procedure
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Barbed | Vaginal Cuff Closure Time | 10.4 minutes | Standard Deviation 5.2 |
| Smooth | Vaginal Cuff Closure Time | 9.6 minutes | Standard Deviation 4.8 |
Dyspareunia
Assessed preoperatively and up to 3 months postop
Time frame: Postoperative
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Barbed | Dyspareunia | Any female dyspareunia reported | 2 participants |
| Barbed | Dyspareunia | Other | 3 participants |
| Barbed | Dyspareunia | Any male dyspareunia reported | 1 participants |
| Barbed | Dyspareunia | Ongoing problem | 0 participants |
| Smooth | Dyspareunia | Other | 0 participants |
| Smooth | Dyspareunia | Ongoing problem | 1 participants |
| Smooth | Dyspareunia | Any male dyspareunia reported | 0 participants |
| Smooth | Dyspareunia | Any female dyspareunia reported | 1 participants |