JPRN-UMIN000009563
Completed
Phase 2
Randomized study comparing simultaneous injection with sequential injection of Fulvestrant - Randomized study of injection methods of Fulvestrant
ConditionsPostmenopausal breast cancer
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Postmenopausal breast cancer
- Sponsor
- Yokohama City University Medical Center
- Enrollment
- 40
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\)Patients who are impossible to be enrolled with psychological diseases or disorder 2\)Inappropriate patients by investigator' decision
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Randomized comparison of two injection techniques for ultrasound-guided supraclavicular block following arthroscopic shoulder surgery; subfascial vs extrafascial injectioDiseases of the musculo-skeletal system and connective tissueKCT0003794Inha University Hospital50
Active, not recruiting
Not Applicable
Randomized trial comparing injection frequency between Aflibercept and Ranibizumab in patients with Central Retinal Vein Occlusion with a treat and extent algorithmCentral retinal vein occlusionTherapeutic area: Diseases [C] - Eye Diseases [C11]EUCTR2014-001047-21-SESankt Eriks Eye Hospital
Recruiting
Phase 3
Investigating the effect of simultaneous infusion of lidocaine and ketamine compared to single infusion of lidocaine and ketamine on neuromonitoring in spine surgeriesIRCT20230204057318N2Shahid Beheshti University of Medical Sciences90
Not yet recruiting
Phase 4
Comparative Randomized ,Single Dose, Two-Way Crossover, Open-label Study to Determine Bioequivlence of Olanzapine 5 mg Orally Disintegrating Tablets Formulations, Zyprexa Zydis (5 mg) and ZOLAN GPO (5 mg), after Oral Administration to Healthy Thai Volunteers under Fasting ConditionsHealthy volunteersTCTR20171204002Pharmacy Service Center, Faculty of Pharmacy, Chiang Mai University30
Completed
Phase 3
A clinical trial comparing low dose versus standard dose of intravenous paracetamol for PDA closure in very premature babiesHealth Condition 1: null- Premature neonates at birthCTRI/2017/10/010012Surya Childrens Medicare Private limited102