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Local Hyperthermia for the Treatment of Cervical Intraepithelial Neoplasias

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Styrktaraðilar
First Hospital of China Medical University

Lykilorð

Útdráttur

Human papillomavirus(HPV) infect epithelial cells and have the capacity to stimulate cell abnormal hyperplasia, especially by those high-risk HPV types. HPV vaccine primarily targeting HPV6/11/16/18 has been available and makes it possible to prevent cervical cancer. However, a large population was left unvaccinated, specifically for those aged ones. In clinic, patients harboring high-risk HPV is quite prevalent in China or other developing nations. Removing the virus and prevention of malignant transformation is required.
Mild local Hyperthermia with a certain temperature range has been successfully used in the treatment of some diseases. It has been utilised in the treatment of some neoplasm, fungal and HPV infections. Investigators' study found that local hyperthermia at 44°C could cleared HPV in more than half of the patients with plantar warts. Investigators also note the fact that in patients with multiple lesions, the clearance of the target lesion is commonly followed by clearance of other distant lesions, a phenomenon suggesting that local hyperthermia could aid in establishing a specific immune response to eliminate HPV.So the purpose of the study is to evaluation local hyperthermia in the treatment of cervical intraepithelial neoplasias grade I and II after 3 months, with positive high-risk type HPVs, and patients with positive testing for high risk HPVs. Appropriate control arms were designed for different conditions.

Lýsing

Mild local Hyperthermia with a certain temperature range has been successfully used in the treatment of some diseases. It has been utilised in the treatment of some neoplasm, fungal and HPV infections. Investigators' study found that local hyperthermia at 44°C could cleared HPV in more than half of the patients with plantar warts. Investigators also note the fact that in patients with multiple lesions, the clearance of the target lesion is commonly followed by clearance of other distant lesions, a phenomenon suggesting that local hyperthermia could aid in establishing a specific immune response to eliminate HPV.So the purpose of the study is to evaluation local hyperthermia in the treatment of cervical intraepithelial neoplasias grade I and II after 3 months, with positive high-risk type HPVs, and patients with positive testing for high risk HPVs. Appropriate control arms were designed for different conditions. One control arm is local hyperthermia at 37°C for 30 mins targeted for CINⅠ, the other control arm is LEEP targeted for CINⅡ. After 3 months, to evaluate the effectivity of local hyperthermia.

Dagsetningar

Síðast staðfest: 01/31/2020
Fyrst lagt fram: 07/21/2017
Áætluð skráning lögð fram: 02/10/2018
Fyrst sent: 02/18/2018
Síðasta uppfærsla lögð fram: 05/21/2020
Síðasta uppfærsla sett upp: 05/21/2020
Raunverulegur upphafsdagur náms: 01/27/2018
Áætlaður aðallokunardagur: 05/07/2020
Áætlaður dagsetningu rannsóknar: 07/31/2020

Ástand eða sjúkdómur

Cervical Intraepithelial Neoplasia
Human Papilloma Virus

Íhlutun / meðferð

Device: local hyperthermia at 37℃ for 30 mins

Device: coniztion of the cervix treatment

Device: Local Hyperthermia at 44℃

Stig

-

Armhópar

ArmurÍhlutun / meðferð
Experimental: Local Hyperthermia at 44℃ for HPV+/CIN-1
Local hyperthermia at 44℃ for 30 mins on cervical region, at days of 1,2,3 and 17, 18. HPV+ and normal cytology or HPV+/CIN-1
Sham Comparator: local hyperthermia at 37℃ for 30 mins
HPV+/CIN-1
Device: local hyperthermia at 37℃ for 30 mins
As a control, for patients with HPV+/CIN-1 or HPV+ with normal cytology, hyperthermia at 37℃ is applied
Active Comparator: coniztion of the cervix treatment
coniztion of cervix for HPV+/CIN2, including LEEP or cold knife coniztion
Device: coniztion of the cervix treatment
For patients with HPV+ / CIN-2
Experimental: Local Hyperthermia at 44℃ for CIN2/HPV+
Local hyperthermia at 44℃ for 30 mins at days of 1,2,3 and 17, 18. HPV+ and CIN2.

Hæfniskröfur

Aldur hæfur til náms 18 Years Til 18 Years
Kyn sem eru hæf til námsFemale
Tekur við heilbrigðum sjálfboðaliðum
Viðmið

Inclusion Criteria:

- 18-65 years old; generally healthy gynecological conditions, normal sexual life; high risk HPV; Cervical biopsy CIN or no cytological changes; signed informed consent

Exclusion Criteria:

- Pregnant woman;local or systematic treatment within 3 months; Comorbidity of other severe gynecological inflammation, infection, or tumor; Comorbidity of other serious illnesses; no guarantee of timely treatment and follow-up

Útkoma

Aðal niðurstöður ráðstafanir

1. clearance rates of HPV [3 months after the last time of treatment.]

to evaluate the clearance rates in different treatment groups 3 month after treatment.

2. scoring atypia by cytology/pathology [3 months after the last time of treatment.]

to evaluate atypia severity score of cervical cells 3 month after treatment.

Aðgerðir vegna aukaatriða

1. viral load measurement [3 months after the last time of treatment.]

to measure the HPV 16 viral load after 3 month of treatment

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