Cervical Carcinoma, Dyspareunia, Endometrial Carcinoma, Ovarian Carcinoma, Vaginal Carcinoma, Vaginal Dryness, Vulvar Carcinoma
Conditions
Brief summary
This randomized pilot trial studies how well fractional carbon dioxide (CO2) laser therapy works in minimizing genitourinary syndrome of menopause (GSM) in gynecological cancer survivors. Fractional CO2 laser therapy may reduce symptoms of GSM in survivors of gynecologic cancers.
Detailed description
PRIMARY OBJECTIVES: I. To conduct a pilot trial to estimate the proportion of gynecologic cancer patients with vaginal dryness or dyspareunia, who will have an improvement in their symptoms with vaginal laser therapy compared to sham treatment based on the Vaginal Assessment Scale (VAS). SECONDARY OBJECTIVES: I. To evaluate toxicity associated with vaginal laser therapy in this population. II. To determine how many women with the defined patient eligibility will complete all treatments. III. To determine the feasibility of the crossover design for potential use in a phase III trial. IV. To determine improvement in objective findings of vaginal atrophy with vaginal laser therapy versus sham treatment. V. To determine improvement in sexual function as measured by Female Sexual Function Index (FSFI), Female Sexual Distress Scale-Revised (FSDS), and scales for sexual satisfaction and behavior with vaginal laser therapy versus sham treatment. VI. To determine improvement in urinary symptoms of urogenital atrophy with vaginal laser therapy versus sham treatment using the Urogenital Distress Inventory (UDI). VII. To demonstrate satisfaction with vaginal fractional CO2 laser therapy. OUTLINE: Patients are randomized in to 1 of 2 arms. ARM I: Patients undergo fractional CO2 laser therapy at 3 time points 30 days apart. ARM II: Patients undergo sham laser therapy at 3 time points 30 days apart. Patients may then crossover to Arm I. After completion of study, patients are followed up at 1 month.
Interventions
PROCEDURELaser Therapy
Undergo fractional CO2 laser therapy
OTHERQuestionnaire Administration
Ancillary studies
PROCEDURESham Intervention
Undergo sham laser therapy
Sponsors
Ohio State University Comprehensive Cancer Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
FEMALE
Healthy volunteers
No
Inclusion criteria
* Women with cervical, endometrial, vaginal, vulvar or ovarian cancer who have completed all cancer related treatment \>= 6 months prior to enrollment * Any form of hysterectomy, including radical hysterectomy permitted * Must have no evidence of recurrent disease on pelvic exam within past 3 months * Radiation therapy is permitted but not required * Patient reported dyspareunia and/or vaginal dryness with severity of \>= 4 on a scale from 0 (none) to 10 (most severe) that has been persistent over \>= 4 weeks and/or the inability to be sexually active due to pain
Exclusion criteria
* Patients with recurrent or metastatic endometrial, vaginal, vulvar, cervical, or ovarian cancer * Pelvic organ prolapse stage II or higher * Prior reconstructive pelvic surgery involving mesh * Hormone replacement therapy or vaginal estrogen therapy within 6 weeks prior to enrollment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in genitourinary syndrome of menopause (GSM) symptoms | Baseline to 12 weeks | Will be assessed by the Vaginal Assessment Scale (VAS). Will be summarized and compared between the treatment arms using a two-sample t-test or a Wilcoxon rank sum test, with a two-sided alternative for each. Will also analyze this endpoint graphically by plotting the VAS scores through time by treatment arm. Additionally, will correlate the scores from the VAS with other validated measures using a Spearman's correlation coefficient in an exploratory manner. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in objective findings of vaginal atrophy | Up to 1 month | Will determine improvement in objective findings of vaginal atrophy with vaginal laser therapy versus sham treatment. |
| Improvement in sexual function by FSFI | Up to 1 year | Will determine improvement in sexual function as measured by Female Sexual Function Index (FSFI) |
| Improvement in sexual function FSDS | Up to 1 year | Will determine improvement in sexual function as measured by Female Sexual Distress Scale-Revised (FSDS) |
| Feasibility as measured by number of patients able to complete 3 study visitis | Up to 1 month | A crossover design to determine the feasibility of the crossover design for potential use in a phase III trial by summarizing the proportion of patients who are unable to tolerate the study treatment prior to completing the 3 treatments |
| Incidence of adverse events | Up to 1 month | Adverse event grading will be done according to the NCI Common Terminology Criteria for Adverse Events version 4.0 (CTCAE) |
| Number of patients complete all treatments | Up to 1 month | Summarize the proportion of patients who are able to tolerate the study treatment and complete the 3 treatments. |
| Satisfaction with vaginal fractional CO2 laser therapy | Up to 1 month | Patients will be asked to rate their satisfaction with the procedure on a likert-type scale of 1-10 with 1 being completely dissatisfied and 10 being extremely satisfied. Participants will be asked to rate their satisfaction on this scale after each treatment and at follow-up. |
| Improvement in urinary symptoms | Up to 1 month | Will determine improvement in urinary symptoms of urogenital atrophy with vaginal laser therapy versus sham treatment using the Urogenital Distress Inventory (UDI). The change in dyspareunia and dryness between baseline (T0) and T4 will be calculated and compared between the treatment and sham arms using a two sample t-test or Wilcoxon rank sum test. |
Countries
United States
Outcome results
None listed