An Observational Study Assessing Effects in Patients With Combination Therapy With Raloxifene/Cholecalciferol

Osteoporosis Clinical Trial

Official title:

An Observational Study Assessing Effects on Quality of Life, Medication Compliance, Treatment Satisfaction in Patients With Combination Therapy With Raloxifene/Cholecalciferol

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04788290
• Other study ID #: HM-RAB-OS-01
• Status: Completed
• Start date: November 6, 2017
• Est. completion date: July 13, 2020

Study information

• Verified date: March 2021
• Source: Hanmi Pharmaceutical Company Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This study examines quality of life and patient satisfaction in postmenopausal women receiving raloxifene to prevent/treat osteoporosis, and vitamin D to reduce risk of fracture using clinical practice data. The purpose of this study is to observe quality of life(QOL), medication compliance and patient satisfaction who got combination therapy with raloxifene/cholecalciferol (raloxifene 60mg + cholecalciferol 800 IU, Rabone D®, Hanmi Pharma, South Korea) for 6 months.

Description:

Preventing bone loss is an important concern for women during post-menopausal period. Menopause significantly speeds bone loss and increases the risk for osteoporosis. This study was to investigate the effectiveness on quality of life (QOL), patient satisfaction in postmenopausal women receiving raloxifene/cholecalciferol combination therapy. In addition, we analyzed adverse events to assess the safety profile of this drug.

This study is a multicenter, prospective, non-critical observational study of women receiving raloxifene/cholecalciferol (raloxifene 60mg + cholecalciferol 800 IU, Rabone D®, Hanmi Pharma, South Korea) combination therapy to treat or prevent postmenopausal osteoporosis. Data will be collected from patients receiving routine treatment at about 105 primary, secondary, or tertiary medical institutions in South Korea. Each subject visits the institution according to the protocol that designed the follow-up visits for six months to examine changes in, and factors influencing quality of life (EQ-5D-5L method), patient satisfaction with efficacy and convenience (questionnaire), and safety. This study will approved by the institutions' IRBs and is in compliance with clinical research ethics regulations.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 3907
• Est. completion date: July 13, 2020
• Est. primary completion date: July 13, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Postmenopausal women who need to prevent/treat osteoporosis

• Subject who got raloxifene/cholecalciferol combination therapy prescription with confirmation by the investigator's medical decision

• Subjects who can consent voluntarily

Exclusion Criteria:

• Patients for whom use of raloxifene/cholecalciferol combination therapy is prohibited

• Pregnant women, nursing women or child-bearing aged females deemed capable of pregnancy

Related Conditions & MeSH terms

• Osteoporosis

Intervention

Other:
• Observational
Rabone D®, Once daily administered per the locally approved product information

Locations

Country	Name	City	State
Korea, Republic of	Hanmi Pharmaceutical Company Limited	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Hanmi Pharmaceutical Company Limited

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The EuroQol EQ-5D	Change and impact factor of quality of life measured with the EuroQol (EQ-5D); EQ-5D-5L is designed to measure health conditions and it consists of 5 questions relating to mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Measuring EQ-5D is performed at each visit.; The EQ-5D-5L consists of descriptive system with 5 dimensions. Each dimension has 5 levels: No problems(1), Slight problems(2), Moderate problems(3), Severe problems(4), and Extreme problems(5).	6 months
Secondary	Medication compliance (Rate of subjects taking more than 80% of the medication)	This study is to learn more about the relationship between quality of life, patient satisfaction and medication compliance. Measuring medication compliance is performed at each visit. The subjects taking more than 80% are defined as compliance group, and the subjects taking less than 80% are defined as non-compliance group. Medication compliance will be compared between compliance group and non-compliance group.	6 months
Secondary	Treatment satisfaction measured with questionnaire (Patient satisfaction)	This study is to learn more about the relationship between quality of life, patient satisfaction and medication compliance. Measuring patient satisfaction is performed at each visit.; Treatment satisfaction is measured with 5 satisfaction degrees(Extremely satisfied, Satisfied, Moderate, Dissatisfied, and Extremely dissatisfied).	6 months
Secondary	Evaluation of clinical laboratory changes (BTM(Bone turnover marker) CTX)	The following laboratory test is performed at each visit.; : CTX (lab unit: e.g. ng/L)	6 months
Secondary	Evaluation of clinical laboratory changes (BTM(Bone turnover marker) NTX)	The following laboratory test is performed at each visit.; : NTX (lab unit: e.g. nM BCE/mM creatinine)	6 months
Secondary	Evaluation of clinical laboratory changes (BTM(Bone turnover marker) BAP)	The following laboratory test is performed at each visit.; : BAP (lab unit: e.g. mcg/L)	6 months
Secondary	Evaluation of clinical laboratory changes (BTM(Bone turnover marker) P1NP)	The following laboratory test is performed at each visit.; : P1NP (lab unit: e.g. µg/L)	6 months
Secondary	Evaluation of clinical laboratory changes (BTM(Bone turnover marker) osteocalcin)	The following laboratory test is performed at each visit.; : osteocalcin (lab unit: e.g. ng/mL)	6 months
Secondary	Evaluation of clinical laboratory changes (25(OH)D level(25-hydroxyvitamin D level)	The following laboratory test is performed at each visit.; : 25(OH)D level(25-hydroxyvitamin D level) (lab unit: e.g. ng/mL)	6 months
Secondary	Reason for medication change	Reason for medication(prior-medication to prevent/treat osteoporosis and concomitant medications) change is collected at each visit.	6 months
Secondary	Evaluation of quality of life changes compared with prior medication regimens	This study is to learn more about quality of life changes compared with prior medication regimens. At visit 1, all subjects conduct questionnaire surveys about quality of life. If there are subjects having prior medication regimens for osteoporosis treatment/prevention, these regimens are classified by medication group to compare and evaluate the change in quality of life after taking combination therapy with raloxifene/cholecalciferol. The prior medications are standardized according to ATC(Anatomical Therapeutic Chemical) classification and analyzed based on level 4 and level 5. Change of EQ-5D index according to prior medication regimens is analyzed with average difference of the sum value.	6 months
Secondary	Occurrence and aspect of adverse events(AEs)	After receiving Rabone D®, new adverse events and detailed information are collected at visit 2 and visit 3.	6 months