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NCT Number: NCT04753073

Treatment of Cervical Intraepithelial Neoplasia (CIN) Grade III With Non-invasive Physical Plasma

The aim of the prospective, unicenter proof-of-principle study is to investigate the anti-neoplastic effectiveness of NIPP against CIN III lesions.

* The aim of this project is to evaluate the potential of a previous NIPP treatment to significantly reduce the invasiveness of the LEEP excision. * Another aim of this study is to investigate cellular / molecular effects of NIPP following the in-vivo treatment of the cervix using molecular biological methods. For this purpose, tissue treated with plasma is taken after defined periods of time by mini biopsy and examined using molecular biological, histological and microscopic methods.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital Tuebingen, Department of Women's Health

Tübingen, 72076, Germany

About this study

Cervical intraepithelial neoplasms (CIN), classified into severity levels CIN I to III, can be precursors to cervical cancer (CC), the world's third most common cancer in women (270,000 deaths / year), which radical therapies are often associated with lifelong severe physical and emotional stress. Cross-sectional studies found a prevalence for CIN of 62 per 1,000 women and incidences of 1.2 (CIN I), 0.8 (CIN II) and 0.7 (CIN III) per 1,000 women per year (highest incidence of CIN between 20 and 24 years) age). The standard therapy for the treatment of CIN III by LEEP excision is associated with an increase in mortality of 17%. CIN III, in particular, is associated with a significant decline in quality of life, psychological well-being and sexual health, although on average only about 12% of CIN III lesions progress to invasive CC. The resulting over-treatment (in around 8-9 out of 10 patients) with invasive procedures is a serious problem for affected women, health care providers and the health economy.

The NIPP treatment is a tissue-sparing, pain-free, easy to carry out and outpatient treatment method without anesthesia and hospitalization. A non-randomized, one-arm feasibility study at the Department of Women's Health (649 / 2017BO1) already showed the effectiveness of a NIPP treatment.

Clinical implications for CIN III:

  • A previous NIPP treatment should significantly reduce the invasiveness of the LEEP excision.
  • If the oncological safety of NIPP treatment is comparable (histological complete remission of CIN III), NIPP is to be established as a safe alternative to LEEP excision in the future.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • Histologically confirmed CIN III
  • Clearly visible transformation zone of the portio and margins of the lesions according to T1 / T2
  • signed written consent

Exclusion criteria

  • Not fully visible transformation zone
  • Indication of an invasive disease
  • Serious cardiovascular diseases
  • Patients who only want to undergo a LEEP excision

Treatment and study plan

Non-invasive physical plasma

Procedure

Treatment with non invasive physical low-temperature plasma

Primary outcomes

  1. Rate of histological complete remission

    Time frame: 8 Weeks

    Rate of histological complete remission of the CIN III at the time of the LEEP excision

Secondary outcomes

  1. Rate of partial histological remission

    Time frame: 8 Weeks

    Rate of partial histological remission of the CIN I / II

  2. Rate of decreased HPV viral load

    Time frame: 8 Weeks

    Rate of decreased HPV viral load in tissues

  3. Pain and quality of life

    Time frame: 8 Weeks

    Pain and quality of life (Freiburg index for patient satisfaction)

    • Pain assessment i) previous to, ii) during, iii) 4 h after, iv) 2 days after, v) 1 week after NIPP treatment, min/max values: 0 - 10, higher scores mean worse outcome
    • Satisfaction assessment, min/max values: 1-6, higher scores mean worse outcome

Sponsors and collaborators

Lead sponsor

University Hospital Tuebingen

Other

Registry information

Acronym: ZGynO_CINIII

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Feb 12, 2021
Registry last updated
Jul 5, 2024

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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