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Recruiting NCT06962644

NCT06962644 Association of Urinary Tract Infection With Preeclampsia During Pregnancy

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Clinical Trial Summary
NCT ID NCT06962644
Status Recruiting
Phase
Sponsor Pakistan Air Force (PAF) Hospital Islamabad
Condition Urinary Tract Infection (Diagnosis)
Study Type OBSERVATIONAL
Enrollment 160 participants
Start Date 2025-01-01
Primary Completion 2025-04-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 35 Years
Study Type OBSERVATIONAL
Interventions
Preeclampsia developed

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 160 participants in total. It began in 2025-01-01 with a primary completion date of 2025-04-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Urinary tract infections (UTIs) are a major clinical issue, especially in pregnant women, due to physiological changes that increase susceptibility. If untreated, UTIs can lead to severe complications like preterm labor and low birth weight. Preeclampsia, a hypertensive disorder affecting 0.2-9.2% of pregnancies, is another leading cause of maternal and fetal complications. The relationship between UTIs and preeclampsia remains controversial, with some studies suggesting an association while others show conflicting results. Research gaps highlight the need for region-specific studies, particularly in Pakistan, where both conditions contribute significantly to maternal and neonatal morbidity. This study aims to investigate the association between UTIs and preeclampsia in pregnant women in Pakistan. It will use a cohort design, enrolling 160 patients (80 with UTIs, 80 without) from the Obstetrics Department of PAF Hospital, Islamabad. Participants will be followed until delivery, with preeclampsia diagnosed based on blood pressure and proteinuria criteria. Data will be analyzed using SPSS to calculate relative risk (RR), with statistical significance set at RR \>1 and p ≤ 0.05. The findings could help improve prenatal care and reduce adverse outcomes in high-risk populations.

Eligibility Criteria

Inclusion Criteria: * Patients attending OPD for routine antenatal checkup * Patients diagnosed with UTI as per operational definitions * Gestational age greater than 20 weeks as per LMP * Age between 18 to 35 years Exclusion Criteria: * History of medical conditions such as: * Diabetes mellitus * Chronic hypertension * Chronic liver or kidney diseases * Chronic pulmonary conditions * History of urological surgical interventions in the past 3 months * History of renal transplants * Patients on immunosuppressive therapy * History of comorbid conditions including: * Diabetes mellitus * Gestational diabetes mellitus * Hypertension * Chronic hepatic diseases * Chronic liver diseases * Chronic pulmonary diseases * Ischemic heart diseases

Contact & Investigator

Central Contact

Wajiha Fatima Resident, MBBS, FCPS (I)

✉ mwajeeha52@gmail.com

📞 +923338747575

Frequently Asked Questions

Who can join the NCT06962644 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 35 Years, studying Urinary Tract Infection (Diagnosis). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06962644 currently recruiting?

Yes, NCT06962644 is actively recruiting participants. Contact the research team at mwajeeha52@gmail.com for enrollment information.

Where is the NCT06962644 trial being conducted?

This trial is being conducted at Islamabad, Pakistan.

Who is sponsoring the NCT06962644 clinical trial?

NCT06962644 is sponsored by Pakistan Air Force (PAF) Hospital Islamabad. The trial plans to enroll 160 participants.

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