TerminatedNot Applicable

Desvenlafaxine Succinate (Pristiq): Postmarketing Surveillance Study Among Filipino Patients

Philippines13 participantsStarted 2012-03

Plain-language summary

This is a non-interventional study to review safety data on administration of desvenlafaxine succinate among Filipino patients with MDD and VMS per usual clinical practice within the first three years post commercial distribution.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: Patients diagnosed with major depressive disorder and vasomotor symptoms secondary to menopause prescribed with desvenlafaxine succinate Exclusion Criteria: Hypersensitivity to desvenlafaxine succinate

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Number of Participants With Treatment-Emergent Adverse Events (TEAEs) or Serious Adverse Events (SAEs), or Discontinuation Due to Adverse Events (AEs)

Timeframe: Week 4 to Week 8

Change From Baseline in Systolic Blood Pressure (BP) and Diastolic BP at Week 4.

Timeframe: Week 4

Change From Baseline in Systolic Blood Pressure (BP) and Diastolic BP at Week 8.

Timeframe: Week 8

Change From Baseline in Heart Rate at Week 4.

Timeframe: Week 4

Change From Baseline in Heart Rate at Week 8.

Timeframe: Week 8

Change From Baseline in Weight at Week 4.

Timeframe: Week 4

Change From Baseline in Weight at Week 8.

Timeframe: Week 8

Trial details

NCT IDNCT01353963

SponsorPfizer

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2012-08

Results submitted2015-12-04

View on ClinicalTrials.gov More Major Depressive Disorder trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Number of Participants With Treatment-Emergent Adverse Events (TEAEs) or Serious Adverse Events (SAEs), or Discontinuation Due to Adverse Events (AEs)

Timeframe: Week 4 to Week 8

Change From Baseline in Systolic Blood Pressure (BP) and Diastolic BP at Week 4.

Timeframe: Week 4

Change From Baseline in Systolic Blood Pressure (BP) and Diastolic BP at Week 8.

Timeframe: Week 8

Change From Baseline in Heart Rate at Week 4.

Timeframe: Week 4

Change From Baseline in Heart Rate at Week 8.

Timeframe: Week 8

Change From Baseline in Weight at Week 4.

Timeframe: Week 4

Change From Baseline in Weight at Week 8.

Timeframe: Week 8