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Transdermal Estrogen Provides Comparable Effectiveness with Desmopressin in Preventing Uremic Bleeding in Chronic Kidney Disease Patients Undergoing Kidney Biopsy: A Randomized, double-blinded controlled trial

Transdermal Estrogen Provides Comparable Effectiveness with Desmopressin in Preventing Uremic Bleeding in Chronic Kidney Disease Patients Undergoing Kidney Biopsy: A Randomized, double-blinded controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20220419012
Enrollment
94
Registered
2022-04-19
Start date
2020-09-14
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

Effectiveness in preventing post-biopsy bleeding complication in CKD patients comparing between transdermal estrogen and desmopressin Uremic bleeding, kidney biopsy, Estrogen, Transdermal estrogen, DDAVP, desmopressin

Interventions

transdermal estrogen 50 mcg of estradiol / 24 hours Climara,0.4 mcg/kg Intravenous desmopressin
Experimental Drug,Active Comparator Drug
Transdermal estrogen,Desmopressin

Sponsors

Kinh Chulalongkorn memorial hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were patients undergoing ultrasound-guided kidney biopsy who were aged above 18 years and estimated glomerular filtration rate (GFR) less than 60 mL/min (calculated using CKD-EPI) with blood pressure less than 140/90 mmHg and hemoglobin more or equal 10 g/dL and normal coagulation parameter (PT and PTT)

Exclusion criteria

Exclusion criteria: patients with history of venous thromboembolism (deep vein thrombosis or pulmonary embolism), history of breast cancer and endometrial cancer, abnormal vaginal bleeding, liver disease and/or history of coronary disease or cerebrovascular disease in previous 1 month before kidney biopsy

Design outcomes

Primary

MeasureTime frame
Postbiopsy bleeding events within 24 hours incidence

Secondary

MeasureTime frame
hematoma size within 24 hours cm2,Hemoglobin level changes within 24 h Hemoglobin level,major bleeding events within 24 h incidence,Platelet function within 24 h PFA-200

Countries

Thailand

Contacts

Public ContactAschariya Wipattanakitcharoen

King chulalongkorn memorial hospital

lingwipat@gmail.com0819022299

Outcome results

None listed

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