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Calcitonin in the Treatment of Fibromyalgia (CALFI)

Primary Purpose

Fibromyalgia

Status
Withdrawn
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
salmon calcitonin
intranasal saline solution plus glycerol
Sponsored by
Unidad de Investigacion en Enfermedades Cronico-Degenerativas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring salmon calcitonin, endorphins, treatment, fibromyalgia

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female patients between 18 and 50 years
  • Fibromyalgia diagnosis (ACR criteria)
  • Must be able to apply the nasal medication
  • Must be able to comply with study visits
  • Must be able to understand informed consent
  • Must be able to answer self-administered questionnaires
  • Must have an active disease(VAS > 60mm)

Exclusion Criteria:

  • Comorbid conditions (i.e. hypothyroidism, diabetes mellitus, etc.)
  • Any disturbance in the nasal tissue
  • Use of concomitant opioid analgesics
  • Contraindication to use salmon calcitonin (allergy, hypocalcemia, hypophosphatemia)
  • Other rheumatic diseases
  • Diagnosis of major depressive disorder

Sites / Locations

  • Hospital General Regional No. 45, IMSS

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

A

B

Arm Description

200 U.I. of intranasal salmon calcitonin

intranasal saline solution and glycerol

Outcomes

Primary Outcome Measures

Functional status as assessed by the Fibromyalgia Impact Questionnaire (FIQ), a self-report inventory developed to measure health status in patients with fibromyalgia

Secondary Outcome Measures

Health related quality of life as assessed by WHO-DAS II, self-report questionnaire. Dolorimetry will be also used

Full Information

First Posted
September 16, 2008
Last Updated
December 3, 2015
Sponsor
Unidad de Investigacion en Enfermedades Cronico-Degenerativas
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1. Study Identification

Unique Protocol Identification Number
NCT00754884
Brief Title
Calcitonin in the Treatment of Fibromyalgia
Acronym
CALFI
Official Title
Phase IV Study of Nasal Salmon Calcitonin in the Treatment of Symptoms and Signs of Fibromyalgia
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Withdrawn
Why Stopped
Study drug was not longer available in our country.
Study Start Date
October 2008 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
February 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Unidad de Investigacion en Enfermedades Cronico-Degenerativas

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether nasal administration of salmon calcitonin is effective and safe in the treatment of symptoms and signs of primary fibromyalgia.
Detailed Description
Fibromyalgia is a common, chronic musculoskeletal disorder that is characterized by widespread pain and tenderness. Fibromyalgia occurs in around 2% of the US general population, is more common in women and is associated with substantial morbidity and disability. Treatment of fibromyalgia has been disappointing; roughly one-third of patients have had a clinically important therapeutic response to medications or no-medicinal treatment, event with the newest drugs reported in the literature. Pathophysiology of fibromyalgia is unknown, but abnormalities in central neurotransmission might play a role. Some studies have shown that salmon calcitonin increases peripheral and central levels of endorphins. Increasing endorphins levels may decrease pain. Then, it is feasible that nasal administered salmon calcitonin may decrease several of the symptoms and signs of patients suffering fibromyalgia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
salmon calcitonin, endorphins, treatment, fibromyalgia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
200 U.I. of intranasal salmon calcitonin
Arm Title
B
Arm Type
Placebo Comparator
Arm Description
intranasal saline solution and glycerol
Intervention Type
Drug
Intervention Name(s)
salmon calcitonin
Other Intervention Name(s)
Miacalcic nasal spray (Novartis Pharmaceutical)
Intervention Description
daily intranasal 200 U.I. salmon calcitonin for periods of 14 days at a time
Intervention Type
Drug
Intervention Name(s)
intranasal saline solution plus glycerol
Other Intervention Name(s)
Nasalub
Intervention Description
daily intranasal (one shot) saline solution plus glycerol for a period of 14 days
Primary Outcome Measure Information:
Title
Functional status as assessed by the Fibromyalgia Impact Questionnaire (FIQ), a self-report inventory developed to measure health status in patients with fibromyalgia
Time Frame
Day 0, Day 14, Day 28 and Day 56
Secondary Outcome Measure Information:
Title
Health related quality of life as assessed by WHO-DAS II, self-report questionnaire. Dolorimetry will be also used
Time Frame
Day 0, Day 14, Day 28 and Day 56

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female patients between 18 and 50 years Fibromyalgia diagnosis (ACR criteria) Must be able to apply the nasal medication Must be able to comply with study visits Must be able to understand informed consent Must be able to answer self-administered questionnaires Must have an active disease(VAS > 60mm) Exclusion Criteria: Comorbid conditions (i.e. hypothyroidism, diabetes mellitus, etc.) Any disturbance in the nasal tissue Use of concomitant opioid analgesics Contraindication to use salmon calcitonin (allergy, hypocalcemia, hypophosphatemia) Other rheumatic diseases Diagnosis of major depressive disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cesar R. Ramos-Remus, M.D., MSc
Organizational Affiliation
Attending Rheumatologist HGR45 and Director UIECD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital General Regional No. 45, IMSS
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44290
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
1865419
Citation
Burckhardt CS, Clark SR, Bennett RM. The fibromyalgia impact questionnaire: development and validation. J Rheumatol. 1991 May;18(5):728-33.
Results Reference
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PubMed Identifier
2306288
Citation
Wolfe F, Smythe HA, Yunus MB, Bennett RM, Bombardier C, Goldenberg DL, Tugwell P, Campbell SM, Abeles M, Clark P, et al. The American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia. Report of the Multicenter Criteria Committee. Arthritis Rheum. 1990 Feb;33(2):160-72. doi: 10.1002/art.1780330203.
Results Reference
background
PubMed Identifier
3549095
Citation
MacIntyre I, Alevizaki M, Bevis PJ, Zaidi M. Calcitonin and the peptides from the calcitonin gene. Clin Orthop Relat Res. 1987 Apr;(217):45-55.
Results Reference
background
PubMed Identifier
3513074
Citation
Szanto J, Jozsef S, Rado J, Juhos E, Hindy I, Eckhardt S. Pain killing with calcitonin in patients with malignant tumours. Oncology. 1986;43(2):69-72. doi: 10.1159/000226336.
Results Reference
background
PubMed Identifier
10584455
Citation
Mystakidou K, Befon S, Hondros K, Kouskouni E, Vlahos L. Continuous subcutaneous administration of high-dose salmon calcitonin in bone metastasis: pain control and beta-endorphin plasma levels. J Pain Symptom Manage. 1999 Nov;18(5):323-30. doi: 10.1016/s0885-3924(99)00081-0.
Results Reference
background
PubMed Identifier
12008161
Citation
Gennari C. Analgesic effect of calcitonin in osteoporosis. Bone. 2002 May;30(5 Suppl):67S-70S. doi: 10.1016/s8756-3282(02)00713-5.
Results Reference
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PubMed Identifier
16575494
Citation
Ofluoglu D, Akyuz G, Unay O, Kayhan O. The effect of calcitonin on beta-endorphin levels in postmenopausal osteoporotic patients with back pain. Clin Rheumatol. 2007 Jan;26(1):44-9. doi: 10.1007/s10067-006-0228-z. Epub 2006 Mar 31.
Results Reference
background
PubMed Identifier
8832998
Citation
Wolfe F. The fibromyalgia syndrome: a consensus report on fibromyalgia and disability. J Rheumatol. 1996 Mar;23(3):534-9. No abstract available.
Results Reference
background
PubMed Identifier
9572636
Citation
Bessette L, Carette S, Fossel AH, Lew RA. A placebo controlled crossover trial of subcutaneous salmon calcitonin in the treatment of patients with fibromyalgia. Scand J Rheumatol. 1998;27(2):112-6. doi: 10.1080/030097498440976.
Results Reference
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Calcitonin in the Treatment of Fibromyalgia

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