Comparison of the incidence of inadequate tissue sampling from uterine curettage in abnormal uterine bleeding between standard and transabdominal ultrasound guided procedure

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20191211001

Enrollment

144

Registered

2019-12-11

Start date

2019-12-10

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Inadequae tissue Inadequate tissue&#44

Interventions

Ultrasound guided while endometrial sampling,Endometrial sampling by standard procedure (blind)

Experimental Device,No Intervention Procedure/Surgery

Ultrasound guided,Blind

Eligibility

Sex/Gender

Female

Age

35 Years to No maximum

Inclusion criteria

Inclusion criteria: Woman age > 35 years with abnormal uterine bleeding

Exclusion criteria

Exclusion criteria: No inform consent, pregnancy, pethidine or analgesic allergy, arrythmia, abnormal sensation, genitourinary neoplasms, coagulopathy, lower urinary tract infection, pelvic inflammatory disease

Design outcomes

Primary

Measure	Time frame
Decrease inadequate tissue in ultrasound guided group Admission time until endometrial sampling Pathology results	—

Secondary

Measure	Time frame
Duration of procedure Between Apply and off the speculum Time	—

Countries

Thailand

Contacts

Public ContactHathaiphat Witsawapaisan

Udonthani hospital

jane.19691@gmail.com0804137132

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026