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Active, Not Recruiting

NCT Number: NCT06756568

The Diagnostic Utility of Ultrasound in Pelvic Inflammatory Disease (PID)

Pelvic inflammatory disease (PID) represents a significant and complex health issue affecting women, particularly those of reproductive age. Characterized by the infection and inflammation of the reproductive organs, PID often results from ascending infections primarily caused by sexually transmitted pathogens, such as Neisseria gonorrhoeae and Chlamydia trachomation. However, it can also be associated with endogenous bacteria or occur following surgical procedures.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Lady Reading Hospital

Peshawar, Khyber Pakhtunkhwa, Pakistan

About this study

The diverse manifestations of PID from asymptomatic cases to acute presentations, pose significant challenges in diagnosis and prompt treatment. Accurate diagnosis is crucial, as untreated infections can lead to severe complications, including infertility, chronic pelvic pain, and ectopic pregnancies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women of reproductive age (18-45 years) presenting with symptoms suggestive of pelvic inflammatory disease (PID).
  • Patients who have been clinically diagnosed with PID based on symptoms such as lower abdominal pain, fever, abnormal vaginal discharge, and tenderness upon pelvic examination.
  • Patients who have undergone preliminary diagnostic tests, such as high vaginal swab (HVS) and urine microscopy, culture, and sensitivity (m/c/s), prior to ultrasound assessment.

Exclusion criteria

  • Pregnant women, due to potential confounding factors in ultrasound findings and differential diagnosis.
  • Patients with chronic pelvic pain not related to acute PID episodes.
  • Patients who do not provide informed consent for participation in the study.
  • Patients with a history of recent pelvic surgery within the last 6 months, as postoperative changes may affect ultrasound findings.

Treatment and study plan

Reduced Morbidity

Diagnostic Test

Early and accurate diagnosis using ultrasound minimizes delays in treatment initiation, thereby preventing complications such as chronic pain and abscess formation. By reducing the severity and duration of the disease, ultrasound contributes to improved patient well-being and a quicker recovery trajectory.

Primary outcomes

  1. ultrasound

    Time frame: 12 Months

    Ultrasound (GE Logiq P7 convex probe.3.5-5MHz) imaging using a curvilinear transducer that provides a broad field of view, commonly used for evaluating abdominal and pelvic organs.

    Doppler flow characteristics which increased blood flow in the pelvic region, especially around the fallopian tubes or ovaries, as detected by color Doppler ultrasound, indicative of inflammation.

Sponsors and collaborators

Lead sponsor

Superior University

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Jan 3, 2025
Registry last updated
Jan 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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