Skip to content

Remaxol® Used in the Treatment of Patients With Gallstone Disease Complicated With Obstructive Jaundice

Observational Study of Efficiency of the Drug Remaxol® (Inosine + Meglumine + Methionine + Nicotinamide + Succinic Acid) Used in the Treatment of Patients With Gallstone Disease Complicated With Obstructive Jaundice

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05928286
Enrollment
286
Registered
2023-07-03
Start date
2022-12-01
Completion date
2025-12-31
Last updated
2026-04-21

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

Conditions

Gallstone Disease, Obstructive Jaundice

Keywords

Gallstone disease, Obstructive jaundice, Remaxol

Brief summary

Obstructive jaundice is observed in 10-80 % of gallstone disease cases. The conventional tactics for the management of patients with obstructive jaundice is to remove biliary hypertension by using endoscopic or minimally invasive methods. The final surgical treatment is performed after jaundice reduction and normalization of hepatic functions. We suppose that the administration of the drug Remaxol (Inosine + Meglumine + Methionine + Nicotinamide + Succinic acid) during the perioperative period shortens jaundice duration and decreases the complications rate.

Interventions

The perioperative infusion of Remaxol® (Inosine + Meglumine + Methionine + Nicotinamide + Succinic acid)

Sponsors

POLYSAN Scientific & Technological Pharmaceutical Company
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Signed informed consent form. 2. Age from 18 to 80 years 3. Diagnosis: Gallstone disease. Cholelithiasis, choledocholithiasis. Obstructive jaundice. 4. Total bilirubin level in the blood in the range from 60 to 246 µmol/l. 5. Jaundice duration according to the patient is not more than 7 days. 6. Scheduled two-staged surgical treatment: 1) common bile duct decompression (endoscopic papillosphincterotomy and endoscopic lithoextraction); 2) laparoscopic cholecystectomy.

Exclusion criteria

1. Presence of other pathology causing jaundice syndrome (tumors, constrictions, etc.). 2. Acute cholangitis. Acute cholecystitis. Acute pancreatitis. 3. History of chronic viral hepatitis, hepatic cirrhosis. 4. Other surgical pathology aggravating the condition and/or requiring treatment. 5. Use in the treatment of drugs containing ademethionine. 6. CHF, functional class III-IV according to NYHA. 7. History of chronic kidney disease and/or creatinine level of more than 130 µmol/l. 8. Respiratory failure. 9. Impairment of consciousness. 10. Diabetes mellitus. 11. Psychic diseases. 12. Autoimmune diseases. 13. Tuberculosis, HIV infection. 14. Pregnancy, lactation.

Design outcomes

Primary

MeasureTime frameDescription
Therapy response rate: decrease of total bilirubin level down to 20.5 µmol/l Visit 3 or decrease in total bilirubin by 70% compared to Visit 1.Up to 2 weeksDecrease of total bilirubin level down to 20.5 µmol/l Visit 3 or decrease in total bilirubin by 70% compared to Visit 1.

Secondary

MeasureTime frameDescription
Therapy response rate: decrease of total bilirubin level down to 61.5 µmol/l and lower by the time of cholecystectomyUp to 2 weeksDecrease of total bilirubin level down to 61.5 µmol/l and lower by the time of cholecystectomy, after successful common bile duct decompression.
Complication rate in the postoperative periodUp to 2 weeksAcute pancreatitis, acute renal failure, acute heart failure, pneumonia, stress hyperglycemia, infectious complications
Total hospitalization duration in days (in case of two-staged surgical treatment).Up to 2 weeksTotal hospitalization duration in days
Total hyperbilirubinemia duration (in days) after the beginning of fluid administration.Up to 2 weeksTotal hyperbilirubinemia duration (in days) after the beginning of fluid administration
Interval (in days) between surgical interventionsUp to 2 weeksInterval (in days) between surgical interventions
Change of hepatic function tests (AST,)Baseline, on the day after surgery, up to 2 weeksChange of hepatic function tests (AST) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of hepatic function tests ( ALT)Baseline, on the day after surgery, up to 2 weeksChange of hepatic function tests (ALT) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of hepatic function test ( AP)Baseline, on the day after surgery, up to 2 weeksChange of hepatic function test ( AP) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of hepatic function test (GGTP)Baseline, on the day after surgery, up to 2 weeksChange of hepatic function test (GGTP) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of hepatic function tests (protein, albumin, fibrinogen)Baseline, on the day after surgery, up to 2 weeksChange of hepatic function tests (protein, albumin, fibrinogen) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of PTIBaseline, on the day after surgery, up to 2 weeksChange of PTI relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of renal function test (urea)Baseline, on the day after surgery, up to 2 weeksChange of renal function test (urea) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Change of renal function test (creatinine)Baseline, on the day after surgery, up to 2 weeksChange of renal function test (creatinine) relative to baseline values, on the day after common bile duct decompression, by the time of cholecystectomy, on the day after cholecystectomy, and on the day of hospitalization termination.
Number of patients whose cholecystectomy was delayed till next hospitalization because of the insufficient dynamics of decrease in bilirubinemia.Up to 2 weeksNumber of patients whose cholecystectomy was delayed till next hospitalization because of the insufficient dynamics of decrease in bilirubinemia.

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 22, 2026