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High intensity focused ultrasound combination with a long period Half GnRH-a for adenomyosis: a prospective cohort study

High intensity focused ultrasound combination with a long period Half GnRH-a for adenomyosis: a prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013167
Enrollment
Unknown
Registered
2017-10-30
Start date
2017-11-01
Completion date
Unknown
Last updated
2017-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

adenomyosis

Interventions

A:HIFU
B:a long period Half GnRha
C:HIFU + a long period Half GnRHa

Sponsors

Anhui Provincial Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Premenopausal women aged between 25 to 50 years; 2. Confirmed adenomyosis by history, examination,CA125, MRI or ultrasound; 3. maxium diameter of adenomyoma is more than 3cm; 4. Receive no other steroid hormone medications within 3 months; 5. Be voluntory to this trial and sign the consent form. ;Inclusion criteria: 1. Premenopausal women aged between 25 to 50 years; 2. Confirmed adenomyosis by history, examination,CA125, MRI or ultrasound; 3. maxium diameter of adenomyoma is more than 3cm; 4. Receive no other steroid hormone medications within 3 months; 5. Be voluntory to this trial and sign the consent form. ;Inclusion criteria: 1. Premenopausal women aged between 25 to 50 years; 2. Confirmed adenomyosis by history, examination,CA125, MRI or ultrasound; 3. maxium diameter of adenomyoma is more than 3cm; 4. Receive no other steroid hormone medications within 3 months; 5. Be voluntory to this trial and sign the consent form. ;Inclusion criteria: 1. Premenopausal women aged between 25 to 50 years; 2. Confirmed adenomyosis by history, examination,CA125, MRI or ultrasound; 3. maxium diameter of adenomyoma is more than 3cm; 4. Receive no other steroid hormone medications within 3 months; 5. Be voluntory to this trial and sign the consent form. ;Inclusion criteria: 1. Premenopausal women aged between 25 to 50 years; 2. Confirmed adenomyosis by history, examination,CA125, MRI or ultrasound; 3. maxium diameter of adenomyoma is more than 3cm; 4. Receive no other steroid hormone medications within 3 months; 5. Be voluntory to this trial and sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Maxium diameter of Uterine is more than 10cm, suspicious malignant transformation; 2. Be allergic to or contraindicated to HIFU, GnRH-a; 3. Be pregnant, with accute genital tract inflamation or gynecological malignant diseases such as ovarian cancer; 4. Receive other steroid hormone medications within 3 months. ;Exclusion criteria: 1. Maxium diameter of Uterine is more than 10cm, suspicious malignant transformation; 2. Be allergic to or contraindicated to HIFU, GnRH-a; 3. Be pregnant, with accute genital tract inflamation or gynecological malignant diseases such as ovarian cancer; 4. Receive other steroid hormone medications within 3 months. ;Exclusion criteria: 1. Maxium diameter of Uterine is more than 10cm, suspicious malignant transformation; 2. Be allergic to or contraindicated to HIFU, GnRH-a; 3. Be pregnant, with accute genital tract inflamation or gynecological malignant diseases such as ovarian cancer; 4. Receive other steroid hormone medications within 3 months. ;Exclusion criteria: 1. Maxium diameter of Uterine is more than 10cm, suspicious malignant transformation; 2. Be allergic to or contraindicated to HIFU, GnRH-a; 3. Be pregnant, with accute genital tract inflamation or gynecological malignant diseases such as ovarian cancer; 4. Receive other steroid hormone medications within 3 months. ;Exclusion criteria: 1. Maxium diameter of Uterine is more than 10cm, suspicious malignant transformation; 2. Be allergic to or contraindicated to HIFU, GnRH-a; 3. Be pregnant, with accute genital tract inflamation or gynecological malignant diseases such as ovarian cancer; 4. Receive other steroid hormone medications within 3 months.

Design outcomes

Primary

MeasureTime frame
dysmenorrhea symptoms;Dysmenorrhea degree;Lesion reduction rate;Menstrual volume;Uterine volume reduction rate;Ablation rate;

Countries

China

Contacts

Public ContactZhao Weidong;Zhao Weidong;Zhao Weidong;Zhao Weidong;Zhao Weidong ;;;;

Anhui Provincial Cancer Hospital;Anhui Provincial Cancer Hospital;Anhui Provincial Cancer Hospital;Anhui Provincial Cancer Hospital;Anhui Provincial Cancer Hospital

victorzhao@163.com;victorzhao@163.com;victorzhao@163.com;victorzhao@163.com;victorzhao@163.com+86 13955105591;+86 13955105591;+86 13955105591;+86 13955105591;+86 13955105591

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026