Study Of The Efficacy And Security Of Ibandronate For Osteoporosis Treatment In A HIV-Infected Patients Cohort
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
This project wills to determine the incidence of osteoporosis in our population of HIV-infected patients and to assess the efficacy and security of ibandronate, whose efficacy in post-menopausal women has already been proved.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Ibandronate Behavioral: Lifestyle modifications |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Study Of The Efficacy And Security Of Ibandronate For Osteoporosis Treatment In A HIV-Infected Patients Cohort |
- Increase in lumbar (L2-4) and femoral (trochanter, femur neck, total femur and hip) t-score bone mineral density [ Time Frame: BL, W24, W48, W72, W96 ] [ Designated as safety issue: No ]
- Adverse events [ Time Frame: BL, W12, W24, W36, W48, W60, W72, W80, W96 ] [ Designated as safety issue: Yes ]
- Lab tests [ Time Frame: BL, W12, W24, W36, W48, W60, W72, W80, W96 ] [ Designated as safety issue: Yes ]
- Related clinical events (bone fractures) [ Time Frame: BL, W12, W24, W36, W48, W60, W72, W80, W96 ] [ Designated as safety issue: Yes ]
- Osteoblastic/Osteoclastic activity, bone formation/reabsorption. [ Time Frame: BL, W12, W24, W36, W48, W60, W72, W80, W96 ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 65 |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Ibandronate + Lifestyle modifications
|
Drug: Ibandronate
Ibandronate endovenous 3 mg every 3 months
Behavioral: Lifestyle modifications
Lifestyle modifications: counseling every 3 months
|
|
2
Lifestyle modifications
|
Behavioral: Lifestyle modifications
Lifestyle modifications: counseling every 3 months
|
Detailed Description:
The lower bone mineral density that has been described in patients with HIV-infection has not meant an increase of long term complications. Nevertheless, it could involve an increase if the associated co-mordibity in the future, taking in care that in general population osteoporosis increases 4 times the pathologic fracture risk. That's why it is necessary to know the real prevalence of osteoporosis in this population of patients so the real dimensions of the problems can be defined.
This project wills to determine the incidence of osteoporosis in our population of HIV-infected patients and to assess the efficacy and security of ibandronate, whose efficacy in post-menopausal women has been already proved. If the quarterly use of endovenous ibandronate obtains equivalent results to those obtained with oral and weekly alendronate in other studies with the same population, its use would be justified because of its posology benefits. The monthly or quarterly administration can improve compliance in patients who are recieving a big quantity of drugs, as HIV infected patients do and who probably have to be treated for life. Moreover, its elimination is renal so there is absence of interactions with antiretroviral drugs what mades of ibandronate a very promising alternative. Finally, there's no risk of digestive intolerance because of its parenteral administration and it has a better posology than oral bifosfonates.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- 18 years old or elder.
- Documented HIV-1 infection, with or without antiretroviral treatment.
- Presence of WHO osteoporosis criteria, defined as t-score under -2.5 in lumbar, hip and/or trochanter. (DEXA in the last 6 months is needed)
- Willing to follow the study protocol.
- Informed Consent signature.
Exclusion Criteria:
- In women, pregnancy or breastfeeding.
- Other possible causes of secondary osteoporosis.
- Creatinin over 2.3mg/mL
- Glomerular filter less than 50 mL/min (estimated through MDRD)
- Alendronate treatment in the last 6 months.
Contacts and Locations| Spain | |
| Germans Trias i Pujol Hospital - Lluita Sida Foundation | |
| Badalona, Barcelona, Spain, 08916 | |
| Principal Investigator: | Eugenia Negredo, MD,PhD | Fundacio Lluita Contra la SIDA |
More Information
No publications provided
| Responsible Party: | LLuita Sida Foundation |
| ClinicalTrials.gov Identifier: | NCT00662077 History of Changes |
| Other Study ID Numbers: | VIH-IBAN |
| Study First Received: | April 17, 2008 |
| Last Updated: | July 31, 2008 |
| Health Authority: | Spain: Ministry of Health |
Keywords provided by Germans Trias i Pujol Hospital:
|
osteoporosis bifosfonates ibandronate |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Osteoporosis Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes |
Immune System Diseases Slow Virus Diseases Bone Diseases, Metabolic Bone Diseases Musculoskeletal Diseases Ibandronic acid Diphosphonates Bone Density Conservation Agents Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on June 18, 2013