Efficacy and Dose Ranging Study of Seroguard

Pharmasyntez114 enrolled

Overview

This trial was a multi-center, double-blind, randomized, parallel group, placebo-controlled, phase II study in adult hospitalized female patients with the confirmed diagnosis of pelvic adhesive disease in Study centres in Russia.

In order to evaluate efficacy and safety of Seroguard, solution for IP administration, a study design meeting the set objectives was selected: prospective, multi-center, double-blind, randomized, parallel group, placebo-controlled study. Given the fact that comparison with placebo is considered the best way to prove efficacy and safety of a drug and that currently there are no drugs with a similar mechanism of action at the pharmaceutical product market, a placebo-controlled, parallel group study design was selected. A randomized, parallel group study design was chosen in order to ensure minimization of a selection bias. Subjects were randomized into four groups (two groups of the test drug and two placebo groups corresponding to the two doses) to enable a comparison of Seroguard administration at two doses. A double-blind study design was selected in order to ensure minimization of an outcome evaluation bias.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

DOUBLE

Enrollment

114

Conditions

Adhesion

Interventions

SeroguardDRUG

Seroguard 0.41 g/L solution

PlaceboDRUG

Saline

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Female patients aged from 18 to 45 years with the confirmed diagnosis of pelvic adhesions having indications for surgery (laparoscopic adhesiolysis). 2. Voluntarily and personally signed and dated Form of Informed Consent. 3. Female patients with pelvic adhesions confirmed by gynecological and ultrasound examination. Exclusion Criteria: 1. Female patients having contraindications to surgical treatment (including acute or exacerbated chronical adnexal inflammation); 2. Body mass index of 30.0 kg/m2 and more; 3. Known hypersensitivity to the test drug components (Seroguard); 4. Pregnancy, breastfeeding or planning a pregnancy during the clinical trial; 5. Refusal to use effective contraception methods throughout the study; 6. Positive HIV, RW, HBV or HCV test result; 7. Alcohol abuse, drug addiction, and toxicomania (except smoking); 8. American Society of Anesthesiologists physical status category III and more (ASA); 9. Purulent process in the abdominal cavity; 10. Disseminated endometriosis; 11. WBC count more than 10\*109/L at the complete blood count; 12. Need of using any drugs during the surgery other than 0.02% chlorhexidine aqueous solution throughout the surgery, as well as the test drug or the placebo (0.9% sodium chloride) administered intraperitoneally in the end of surgery. 13. Concomitant diseases that may require conversion of the surgical intervention by other indications; 14. Type I or II diabetes mellitus; 15. Deep vein thrombosis and/or PATE at the screening or in the medical history; 16. Renal impairment (glomerular filtration rate less than 60 mL/min/1.73 m2 assessed by the CKD-EPI equation); 17. Liver disorders defined as more than 2-fold rise of the upper limit of normal of one of the following enzymes: ALT, AST, GGTP, AP, or more than 2-fold total bilirubin increase; 18. Myocardial infarction within 6 months before screening; 19. Any concomitant diseases accompanied by heart failure; 20. Clinically significant ECG changes (as to the investigator's opinion); 21. Any concomitant diseases accompanied by respiratory failure; 22. Any oncological disease within 3 years before enrollment into the study; 23. Systemic inflammatory diseases; 24. Diseases associated with chronic hemorrhages; 25. Blood diseases (anemias of any origin, hemoglobinopathies, inherited and acquired coagulopathies, hemostasis disorders, thrombocytopenias, and thrombocytopathias, any hemoblastoses); 26. Any other disease that, in the investigator's opinion, may affect study results or present an additional threat to well-being of a patient after administration of the study drug; 27. Use of anticoagulants, antiaggregants (except for acetylsalicylic acid at the dose of less than 325 mg/day) at the moment of inclusion into the study or planning to do so during the study; 28. Use of drugs with pronounced hemato-, hepato-, or nephrotoxic action, drugs of biological origin; 29. Need to administer cytostatics, systemic glucocorticosteroids, and other immunosuppressive agents during the patient's participation in the study. 30. Participation in any other clinical trial within 30 days before screening; 31. Contraindications to MRI (presence of implants or implanted electronic devices); 32. Impossibility or inability to comply with the requirements of the protocol, including for physical, psychic or social reasons, in the investigator's opinion.

Locations (14)

Outcomes

Primary Outcomes

Number of Participants With Reduction of Adhesions Number by 3 or More

The number of adhesions according to the first MRI data was compared to the number according to the data of second MRI

Time frame: 30±4 days after surgical intervention

Secondary Outcomes

Change in Thickness of Pelvic Adhesions

The change from baseline was defined. It was evaluated by comparing baseline MRI data and repeated MRI data. Results were estimated according to scale from 0 to 3 where 0 - no adhesions, 1 - thin (filmy or filiform), 2 - marked, 3 - marked with an impaired passage through organs involved.