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CavatermTM vs TCRE in Women With DUB

Multicenter Randomized Clinical Trial to Evaluate the Safety and Effectiveness of Cavaterm TM Thermal Balloon Endometrial Ablation in Women With Dysfunctional Uterine Bleeding Compared to Transcervical Resection of the Endometrium (TCRE)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00549159
Enrollment
158
Registered
2007-10-25
Start date
2007-10-31
Completion date
2009-10-31
Last updated
2008-05-22

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

Conditions

Dysfunctional Uterine Bleeding

Keywords

menorrhagia, dysfunctional uterine bleeding, endometrial ablation

Brief summary

The purpose of study is to compare the treatment success in the study groups.

Detailed description

Study success will be defined as reduction of uterine bleeding evaluated by number of patients obtaining amenorrhea, hypomenorrhea or eumenorrhea quantified by PBLAC\<75.

Interventions

Thermal balloon endometrial ablation

DEVICETranscervical Resection of the Endometrium

Transcervical resection of the endometrium

Sponsors

Pnn Medical A/S
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
30 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Willingness and adequate mental capacity to sign written, informed consent * Willingness to adhere to study plan regarding control visits and recording of PBLAC * \> 30 years old * Pre-menopausal as determined by FSH ≤30 * Agree not to use hormonal contraception or any other intervention for bleeding during study * Suitable for local and/or general anesthesia * A minimum PBLAC score of ≥ 150 for three months prior to study enrollment; OR PBLAC score 150 for one month for women who 1) had at least 3 (documented) prior months of failed medical therapy; 2) had a contraindication to medical therapy; or 3) refused medical therapy * Uterine cavity sound measurement ≥ 4 cm and ≤ 10 cm.

Exclusion criteria

* Presence of bacteriaemia, sepsis, or other active systemic infection * Active pelvic inflammatory disease * Clotting defects or bleeding disorders * Unwillingness to use a non-hormonal birth control post-ablation * Desire for future fertility * Abnormal cavity as confirmed by hysteroscopy, transvaginal ultrasound or HSG e.g. large fibroids, septum etc. Small submucosal fibroids defined as \< 2 cm are in this context not considered abnormal. * Any condition leading to possible uterine wall weakness with total wall thickness \< 15 mm e.g. at c.section, postmyomectomy scars etc. In case of uniform uterine wall the wall thickness at the fundus should be measured. * Premalignant or malignant uterine condition within the last five years as confirmed by histology * Pregnancy * Cervical length \> 6 cm. * Uterine cavity \>30 ml defined as balloon can be filled with 30ml glucose solution without reaching the target pressure of 240 mmHg. (These patients may still be treated as planned but will be withdrawn from the study and their data will be analysed separately. The patients will be recorded as screening failures). * Previous ablation or subtotal hysterectomy

Design outcomes

Primary

MeasureTime frame
Reduction of uterine bleeding evaluated by number of patients obtaining amenorrhea, hypomenorrhea or eumenorrhea quantified by PBLAC<7512 months

Secondary

MeasureTime frame
SF-12, Patients Wishes and Expectations questionnaire, adverse events, need for re-treatment12 months

Countries

China

Contacts

Primary ContactYanhong Yu, Prof.
yuyh20050712@hotmail.com+862061641017
Backup ContactNan Liu, MD
annan0103@yahoo.com.cn+8613889903451

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026