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Study reference: NCT07273851. HopeStage can help you review the study, but cannot decide medical eligibility.
CompletedNCT07273851
Comparison of Propofol and Ketofol as Induction Agents for Electroconvulsive Therapy
This study is completed. It focuses on depression and currently lists study information in Pakistan.
DepressionOtherFrom 18 Years to 65 Years
Key information made simple
This study exists to compare options and see whether a therapy or guided support program offers something meaningfully different. Researchers are trying to understand how people respond to a therapy or guided support program in practice and what may need to be adjusted. For people living with Depression, small gains in stability can make a meaningful difference over time. If the findings are useful, they could help future care become more targeted, practical, and easier to trust. Taking part helps build the evidence that can improve understanding and care for others over time.
Your next step
The official record suggests in-person participation through a hospital, with sites including Department of Anesthesia, Fauji Foundation Hospital, Rawalpindi, Pakistan in Rawalpindi. Participation appears to involve assessments along with scans or samples to help researchers understand patterns more clearly. The main fit is usually meeting the main study requirements, while common reasons not to take part include pregnancy or breastfeeding and other treatments that could interfere with the study. The official record does not list a formal phase, which usually means this is focused more on feasibility, delivery, or support than a standard drug-development stage.
Questions to ask before joining
- What are the exact eligibility criteria, and what could exclude someone?
- How many visits, assessments, or follow-ups are expected, and over what period?
- What risks, side effects, practical burdens, or alternatives should be understood first?
- Who should be contacted to confirm locations, timing, compensation, and next steps?
Things to check before joining
- Sponsor
- Fauji Foundation Hospital
- Sponsor type
- Hospital / academic medical center
- Main activity
- behavioral or lifestyle intervention
- Intervention
- Not available
- Time commitment
- long follow-up or multiple visits
- Study phase
- Not available
- Enrollment
- Not available
- Recruitment status
- Completed
- Source
- Official registry link
Key study information
- Official title
- Comparison of Propofol and Ketofol as Induction Agents for Electroconvulsive Therapy
- Condition
- Major Depressive Disorder
- Study status
- Completed
- Sponsor / lead affiliation
- Fauji Foundation Hospital
- Location / country
- Pakistan
- Registry
- ClinicalTrials.gov
- External trial ID
- NCT07273851
Why this study may matter
This study may matter because it adds public evidence around depression. HopeStage presents it as a starting point for understanding the study, checking the official source, and preparing questions with a care team.
For you
Taking part may help clarify how this condition is measured or understood.
It requires regular visits and structured follow-up.
Requires travel, with in-person participation in Pakistan.
Registry reference
This page links back to the public source record so people can verify details directly with the registry and research team.
If you want the full study description, eligibility criteria, locations, and sponsor information in the original format, this is the place to check before taking the next step.
- Official title
- Comparison of Propofol and Ketofol as Induction Agents for Electroconvulsive Therapy
- Source
- ClinicalTrials.gov
- Official registry link
- Open official registry
- External trial ID
- NCT07273851
Not medical advice
Information from public sources. Are you the study sponsor? Contact us to update this page: hi@hopestage.com
Questions about this study
What is Comparison of Propofol and Ketofol as Induction Agents for Electroconvulsive Therapy?
This study is exploring behavioral or lifestyle intervention for people with depression. Participants may complete study visits, assessments, or follow-up activities defined by the research team. Direct benefit is not guaranteed.
Who is behind this study, and what type of sponsor is it?
This study is sponsored by Fauji Foundation Hospital. Based on the sponsor name or official registry information, it appears to be a hospital or academic medical center. You should verify the details in the official registry record.
What does participation involve, what phase is it, and what should I ask about safety?
This study may involve behavioral or lifestyle intervention, study visits, and assessments. The time commitment is long follow-up or multiple visits. The study phase is not available in HopeStage data. Check the official source record to see whether a phase is listed. Enrollment is not available in HopeStage data. HopeStage cannot say whether a study is safe or right for you. Before joining, ask the research team about possible risks, time commitment, visits, side effects, compensation, safety monitoring, and whether participation may affect your current care.
Where can I verify the study details?
Use the official source record linked on this page to check the full study description, recruitment status, eligibility criteria, locations, sponsor information, phase, enrollment, contact details, and any listed risks or requirements.
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