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Safety and Efficacy of Intravenous Magnesium Sulfate in Modulating Changes in Symptoms and Divalent Cation Levels Associated With Foscavir Therapy: A Phase IV Randomized, Double-Blind, Placebo-Controlled, Cross-Over, Pilot Study

Safety and Efficacy of Intravenous Magnesium Sulfate in Modulating Changes in Symptoms and Divalent Cation Levels Associated With Foscavir Therapy: A Phase IV Randomized, Double-Blind, Placebo-Controlled, Cross-Over, Pilot Study

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002146
Enrollment
12
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cytomegalovirus Infections, HIV Infections, Hypocalcemia

Keywords

Infusions, Intravenous, Foscarnet, Cytomegalovirus Infections, Acquired Immunodeficiency Syndrome, Magnesium Sulfate, Magnesium Deficiency, Hypocalcemia

Brief summary

To determine whether acute ionized hypomagnesemia and hypocalcemia immediately following foscarnet infusions can be lessened or eliminated by prior infusion of magnesium sulfate. To determine whether reductions in ionized magnesium, ionized calcium, and parathyroid hormone levels following foscarnet infusions are lessened by preinfusion of magnesium sulfate. To evaluate the safety of intravenous magnesium sulfate prior to foscarnet infusion by monitoring blood pressure, heart rate, and heart rhythm. To characterize the effect of magnesium sulfate on foscarnet blood levels and urinary excretion of calcium, magnesium, phosphate, and foscarnet.

Detailed description

Patients are randomized to one of four treatment groups. Intravenous foscarnet is administered for 4 days. Patients receive one of three doses of magnesium sulfate or placebo in normal saline according to one of four schedules. Sequence of doses will differ for each group.

Interventions

DRUGMagnesium sulfate
DRUGFoscarnet sodium

Sponsors

Astra USA
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have: * AIDS by CDC criteria. * Documented CMV disease. * Tolerance of foscarnet dose of 90 mg/kg bid. * Normal serum calcium, serum creatinine, and serum phosphate.

Exclusion criteria

Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Known allergy to Foscarnet. * In extremis or incapacitated because of underlying illness (e.g., comatose or tracheally intubated). * Volume depletion. Concurrent Medication: Excluded: * Nephrotoxic drugs such as IV pentamidine, amphotericin B, aminoglycosides, and cisplatin. * Other investigational drugs that affect metabolic balance, such as human growth hormone. * Oral or parenteral magnesium and calcium supplementation. Patients with the following prior condition are excluded: History of heart block.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026