Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Steroid Treatment for Sickle Cell Pain Crisis
This study is currently recruiting participants.
Verified by Baylor College of Medicine, December 2005
Sponsored by: Baylor College of Medicine
Information provided by: Baylor College of Medicine
ClinicalTrials.gov Identifier: NCT00263562
  Purpose

The painful episode is the most common problem experienced by children with sickle cell disease. Although various treatments are available during painful episodes, the medication most commonly given for pain is a pain medication such as morphine. Fluids are also used. Even with these treatments, many children still have severe pain that is difficult to control. In addition to pain medications, there are other medications that may be useful. Methylprednisolone (solumedrol) and prednisone are a group of medications called steroids that may be helpful for painful episodes. These medications are known to lower the amount of inflammation (this means swelling, tenderness, and soreness) in the body. Because this medication may help with your pain, you are being asked to be a part of this study. These types of medications are used in other illnesses such as asthma, especially during times when the illness has gotten worse.

The main purpose of this study is to see if the methylprednisolone and prednisone will lower the amount of pain and the length of hospital stay.

In addition to the pain medication you will normally receive, you will be assigned to one of 2 groups: 1) the experimental group with the active form of the medicine, or 2) a comparison group without the active form of the medicine. In either group, you will still receive all of the treatments you would normally receive for a painful episode, including pain medicines and fluids. You and your doctors will not know what group you will be assigned.

If you decide to be a part of the study the following will happen:

For the first 5 days, you will be asked to: 1) describe your current pain (0=no pain to 10=a lot of pain), worst pain (0=no pain to 10=a lot of pain), least pain (0=no pain to 10=a lot of pain), and the amount of pain relief (0=no relief to 10=complete relief); 2) describe any signs or symptoms you feel, including filling out a pain scale form each day; 3) and take the medicines for 5 days, either at home or when in the hospital. Thirty days after the study, a study researcher will call and will ask questions about your pain, any painful episodes, and any medications you had. If you are discharged home sooner than 5 days after the start of the study, research staff will call you to ask you these questions, remind you to fill out your pain forms, and remind you to take your medicine. If you are discharged home, you will be given pain scales to fill out each day at home.


Condition Intervention Phase
Sickle Cell Disease
Vaso-Occlusive Crisis
Drug: Methylprednisolone plus prednisone taper
Phase III

Genetics Home Reference related topics: sickle cell disease
MedlinePlus related topics: Sickle Cell Anemia
Drug Information available for: Methylprednisolone Prednisone
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Randomized Trial of High-Dose Intravenous Methylprednisolone and Steroid Taper for Vaso-Occlusive Crises in Sickle Cell Disease

Further study details as provided by Baylor College of Medicine:

Primary Outcome Measures:
  • The primary objective of this study is to determine whether the use of high-dose methylprednisolone followed by steroid taper decreases the duration of hospitalization and severity of pain in VOC of sickle cell disease.
  • Primary Hypothesis: The experimental group treated with high-dose methylprednisolone and steroid taper plus conventional therapy will have a lesser duration and and lower severity of pain in VOC than the control group.

Secondary Outcome Measures:
  • 1) to determine whether this methylprednisolone regimen will decrease the number of inpatient admissions.
  • 2) to examine the number and type of complications and side effects (including infection, hypertension, and GI bleeding)
  • 3) to determine rate of recurrent episodes of pain within one month of treatment.
  • 4) to determine whether the amount of analgesic used will decrease during the hospitalization.

Estimated Enrollment: 80
Study Start Date: December 2005
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   8 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Sickle cell and acute pain
  • Age 8 and up
  • English or Spanish-speaking

Exclusion Criteria:

  • Fever > 101
  • Acute chest syndrome or pneumonia
  • Other SS complications (sequestration, aplastic crisis)
  • Other explanation for pain (chronic, AVN, surgical)
  • History of GI bleeding, HTN, or hyperglycemia/DM
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00263562

Contacts
Contact: Cara B Doughty, MD 832-824-5557 cbdought@texaschildrenshospital.org
Contact: Charles Macias, MD, MPH 832-824-5416 cmacias@bcm.tmc.edu

Locations
United States, Texas
Texas Childrens Hospital Recruiting
Houston, Texas, United States, 77030
Contact: Troy Bush     832-824-5459     tbush@bcm.tmc.edu    
Sponsors and Collaborators
Baylor College of Medicine
Investigators
Principal Investigator: Charles Macias, MD, MPH Baylor College of Medicine
  More Information

Study ID Numbers: H-17689
Study First Received: December 8, 2005
Last Updated: December 8, 2005
ClinicalTrials.gov Identifier: NCT00263562  
Health Authority: United States: Institutional Review Board

Keywords provided by Baylor College of Medicine:
Sickle cell disease
vaso-occlusive crisis
steroid treatment

Study placed in the following topic categories:
Prednisone
Hematologic Diseases
Methylprednisolone
Anemia
Anemia, Hemolytic
Methylprednisolone acetate
Prednisolone acetate
Pain
Sickle cell anemia
Anemia, Hemolytic, Congenital
Genetic Diseases, Inborn
Hemoglobinopathies
Prednisolone
Hemoglobinopathy
Anemia, Sickle Cell
Methylprednisolone Hemisuccinate

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Gastrointestinal Agents
Antiemetics
Neuroprotective Agents
Protective Agents
Glucocorticoids
Hormones
Pharmacologic Actions
Autonomic Agents
Therapeutic Uses
Peripheral Nervous System Agents
Central Nervous System Agents

ClinicalTrials.gov processed this record on January 16, 2009