Clinical trial · Interventional
Oxybutynin Chloride in Managing Hot Flashes
A Phase III, Double-Blind, Controlled Trial of Oxybutynin in the Management of Hot Flashes
NCT02961790CI-TRIAL-00042827completedPhase 3Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This randomized phase III trial studies how well oxybutynin chloride works in managing hot flashes in patients who are not candidates for, or not interested in hormone replacement therapy. Previous studies have shown that oxybutynin is effective in managing hot flashes, however doses used in prior studies have resulted in side effects. This trial is evaluating lower doses of oxybutynin with the goal of determining if they are efficacious with less side effects. ADAM-VTE
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Carcinoma | Breast Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Ductal Breast Carcinoma In Situ | Breast Ductal Carcinoma In Situ | ALIAS | 0.90 |
| Hot Flashes | — | UNRESOLVED | — |
| Lobular Breast Carcinoma In Situ | Breast Lobular Carcinoma In Situ | ALIAS | 0.90 |
| No Evidence of Disease | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Oxybutynin Chloride | Drug | — | UNRESOLVED |
| Placebo | Other | — | UNRESOLVED |
| Quality-of-Life Assessment | Other | — | UNRESOLVED |
| Questionnaire Administration | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (4)
- type
- EXPERIMENTAL
- label
- Group I (low-dose oxybutynin chloride)
- description
- Patients receive lower dose oxybutynin chloride PO BID on days 8-49 in the absence of unacceptable toxicity.
- interventionNames
- Drug: Oxybutynin Chloride
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
- type
- PLACEBO_COMPARATOR
- label
- Group II (low-dose placebo)
- description
- Patients receive lower dose placebo PO BID on days 8-49 in the absence of unacceptable toxicity.
- interventionNames
- Other: Placebo
- Other: Quality-of-Life Assessment
- Other: Questionnaire Administration
- type
- EXPERIMENTAL
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * History of breast cancer, ductal breast carcinoma in situ (DCIS), or lobular carcinoma in situ (LCIS) (currently without evidence of malignant disease) OR a concern about taking estrogen for fear of breast cancer * Bothersome hot flashes (defined by their occurrence of \>= 28 times per week and of sufficient severity to prompt the patient to seek therapeutic intervention) * Presence of hot flashes for \> 30 days prior to study entry * Ability to complete questionnaire(s) by themselves or with assistance * Eastern Cooperative Oncology Group (ECOG) performance status (PS) = 0, 1 * Ability to provide informed written consent * Life expectancy \>= 6 months * Willing to work with the enrolling institution for follow-up (during the active monitoring phase of the study) Exclusion Criteria: * Any of the following current (=\< 4 weeks prior) or planned therapies: * Antineoplastic chemotherapy (anti-HER2 agents allowed) * Androgens * Estrogens (any delivery route) * Progestogens * Tamoxifen, raloxifene and aromatase inhibitors are allowed, but patient must have been on a constant dose for at least 28 days and must not be expected to stop the medication during the study period * Selective serotonin reuptake inhibitors (SSRIs)/serotonin?norepinephrine reuptake inhibitors (SNRIs), when being used for hot flash management or other indications such as depression, is allowed, assuming the dose will remain unchanged for the study duration * Gabapentin/pregabalin, when being used for hot flash management (use for other indications, such as pain, is allowed, assuming the dose will remain unchanged for the study duration) * Clonidine * Agents with known potent anticholinergic activity; agents with mild-moderate anticholinergic activity are allowed * Prior use of oxybutynin during the period in which patient has had hot flashes * Pregnant women * Nursing women * History of any of the following contraindications to oxybutynin: * Uncontrolled gastroesophageal reflux disease (GERD) despite appropriate therapy; if patient has history of GERD, but symptoms are well-controlled with medical treatment, patient is eligible * Ulcerative colitis * Narrow-angle glaucoma * Urinary retention * Hypersensitivity to oxybutynin or any other components of the product * Current uncontrolled hyperthyroidism * Coronary heart disease (angina or prior myocardial infarction) * Congestive heart failure * Symptomatic cardiac arrhythmias * Current uncontrolled hypertension * Myasthenia gravis * Dementia
References
Publications (0)
Data not yet available
No reference posted for this study.