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NCT07897786Toborzás még nem indult

Clinical Audit of Cervical Cytology Services in an Early Cancer Detection Unit

Clinical Audit of Cervical Cytology Services in an Early Cancer Detection Unit: Prospective Evaluation of the Screening Pathway From Pap Smear to Definitive Management

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. okt. 27.

Rövid összefoglaló (regiszter, angolul)

Cervical cancer is largely preventable when precancerous changes are detected and treated early. However, an effective screening program requires not only collecting a screening test, but also ensuring seamless continuity across the entire care pathway, including adequate specimen collection, accurate laboratory reporting, prompt referral, timely colposcopy, biopsy confirmation, treatment, and follow-up. Delays or breakdowns at any stage can increase the risk of disease progression. This prospective observational clinical audit aims to evaluate the quality, timeliness, and continuity of cervical cytology services at the Early Cancer Detection Unit, Women's Health Hospital, Assiut University. Women attending the unit who are eligible for cervical screening will be invited to participate. Because this is an observational audit of standard healthcare services, all examinations, tests, and treatments (such as Pap smears, colposcopies, cervical biopsies, and excisional or ablative therapies) are performed strictly according to routine clinical indications and standard management guidelines. No experimental interventions or tests will be administered. The study will prospectively monitor participants along the clinical pathway to evaluate: * The rate of adequate Pap smear specimens and distribution of cytological findings. * Time intervals between screening, cytology results, specialty referral, colposcopy examination, histopathological diagnosis, and definitive treatment. * Rates of completed referrals, colposcopy appointments, biopsy confirmations, and definitive treatments. * Reasons for delayed appointments, missed visits, or loss to follow-up through clinical record reviews and routine patient contact. The findings will help identify patient, provider, and health-system factors contributing to care gaps, providing evidence-based quality indicators to enhance the efficiency and clinical performance of cervical screening services.

Állapot (regiszter)
Toborzás még nem indult
Vizsgálattípus
Megfigyeléses
Résztvevők száma
500 (tervezett)
Első benyújtás
2026. okt. 20.
Kezdés
2026. nov.
Elsődleges befejezés
2027. nov.
Fő szponzor
Assiut University
Betegségek
Méhnyakrák
NCT-szám
NCT07897786

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 500
  • 2026. nov. és az elsődleges befejezés (2027. nov.) között
  • Nincs megadott helyszín, ország nélkül
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

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Korábbi kezelés

  • Prior history or confirmed diagnosis of invasive cervical cancer at the time of enrollment.
  • Previous total hysterectomy with complete removal of the cervix where cervical cancer screening is not clinically indicated.

Egyéb

  • Refusal to participate in the study.
  • Transfer of clinical care to another healthcare facility where sufficient outcome and follow-up information cannot be obtained.

Kiket keres a vizsgálat

  • Women attending the Early Cancer Detection Unit who are eligible for cervical cytology (Pap smear) according to institutional screening policy.
  • Willingness and ability to provide written informed consent to participate.
  • Feasibility of prospective documentation of screening, referral, diagnostic, treatment, and follow-up data.
  • Women with abnormal cytology who require further clinical assessment and agree to be followed through the clinical pathway until definitive management or study completion.

Életkor a regiszterben: 18 év – - · Nem: csak nők

A teljes feltétellista: ClinicalTrials.gov

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