Paroxetine Versus Placebo for Vasomotor Symptom Management in Surgical Menopause (MENOXTINA)

Universidad Nacional Autonoma de Honduras

Status and phase: Completed; Phase 2

Conditions: Menopause Surgical; Menopause Syndrome; Hot Flashes

Treatments: Drug: Paroxetine; Dietary Supplement: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT06763484

PGO-UNAH-48-2-2025

Details and patient eligibility

About

evaluate the efficacy of paroxetine in the management of vasomotor symptoms in patients with surgical menopause, in order to seek an alternative therapy to hormone therapy, which is associated with proinflammatory and procoagulant effects that increase the risk of thrombosis and is therefore contraindicated in people with diabetes mellitus, chronic arterial hypertension and patients with a history of thromboembolism

Full description

Vasomotor symptoms that occur in the peri-menopausal and postmenopausal period are experienced by 80% of women and can greatly affect the quality of life by temporarily interrupting daily activities. These symptoms are experienced early in our study population who are induced to early menopause by undergoing surgical procedures such as total abdominal hysterectomy plus bilateral salpingo-oophorectomy.

Due to the controversy that exists about the use of hormone replacement therapy, in recent years different alternative therapies have been proposed for the management of these symptoms, mainly for those patients who have contraindications for hormone therapy. For this reason, the use of non-hormonal therapy has been investigated.

Since there are women who have contraindications to conventional therapy such as patients with cardiovascular and thrombosis risks, there is a need to search for new alternative therapies such as selective serotonin reuptake inhibitors, specifically paroxetine, so with our study we seek to evaluate how effective paroxetine is in reducing vasomotor symptoms and thus provide an alternative to this type of patients.

Enrollment: 90 patients

Sex: Female

Ages: 18 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patients with surgical menopause attending IHSS outpatient clinic.
• Patients with surgical menopause with presence of hot flashes and night sweats.
• Surgical menopausal patients with episodes of anxiety and palpitations.
• Patients with surgical menopause who receive treatment for 6 months with Paroxetine.
• Patients who after reading and explanation of the Informed Consent agree to participate voluntarily.

Exclusion criteria

• Patients medicated with psychotropic drugs, including all sedatives and hypnotics.
• Patients under treatment with Menopausal Hormone Therapy.
• Patients with impaired hepatic or renal function.
• Patients with unstable heart disease.
• Patients with a history of self-destructive behaviors.
• Patients with a history of clinical diagnosis or treatment for depression or any other psychiatric disorder (including substance abuse or alcohol disorders) and any other ongoing medical condition.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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90 participants in 2 patient groups, including a placebo group

Paroxetine

Experimental group

Description:

20mg Paroxetine once daily for 12 weeks

Treatment:

Drug: Paroxetine

Placebo

Placebo Comparator group

Description:

1 placebo capsule containing starch

Treatment:

Dietary Supplement: Placebo