Quality of Life of Patients With Pregnancy Related VTE

Health, Subjective Clinical Trial

Official title:

Pregnancy-related VTE; Quality of Patients' Lives

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04936373
• Other study ID #: Deanship Academic Research-T
• Status: Completed
• Start date: October 1, 2020
• Est. completion date: March 2, 2021

Study information

• Verified date: December 2023
• Source: University of Jordan
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A retrospective study of the quality of life and problems experienced by patients who developed pregnancy related VTE. It involves patients seen at JUH in 2012-2020. A questionnaire will be filled by those patients and any other patients in Jordan. It was translated to an Arabic form from EQ-5D, VEINES-QOL/SYM questionnaire and PEmb-QoL. The quality of their lives will be assessed and the problems encountered are going to be analyzed to try to find some solutions. This project is going to be a national research project with the efforts to try to find common platforms for those patients and nidus to establish a national support group.

Description:

Retrospective study and analysis using a questionnaire which will be distributed to patients. The patients' data and contact details (phone numbers, whatsApp, email address…) will be collected from their clinical records at the JUH hospital. The period 2012-2020 will be covered. The questionnaire link is; file:///C:/Users/user/Downloads/QoL-post-VTE-during-pregnancy-5.pdf and file:///C:/Users/user/Downloads/arabic%20questionnaire%20last%201.pdf

Recruitment information / eligibility

• Status: Completed
• Enrollment: 112
• Est. completion date: March 2, 2021
• Est. primary completion date: January 20, 2021
• Gender: Female
• Age group: 18 Years to 49 Years

Eligibility

Inclusion Criteria:

• pregnancy related event
• confirmed diagnosis by an objective diagnostic tool (Duplex ultrasonography, CT pulmonary angiography, spiral CT scan or ventilation perfusion scan)
• consent (acceptance) to participate was obtained
• alive patients

Exclusion Criteria:

• death
• an objective diagnostic tool could not be found to confirm the diagnosis
• their event was not related to pregnancy
• refusal to participate

Related Conditions & MeSH terms

• Health, Subjective

Locations

Country	Name	City	State
Jordan	Al-Husban University Naser	Amman
Jordan	The University of Jordan	Amman

Sponsors (1)

Lead Sponsor	Collaborator
University of Jordan

Country where clinical trial is conducted

Jordan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	leg pain	limited mobility (difficulty walking, climbing stairs, bending, kneeling, squatting)	6 months
Primary	Breathlessness	daily activities at work, home or social activities	6 months
Primary	difficulties completing duties at work	Cut down the amount of time you spent on work or other activities , Accomplished less than you would like	6 months