A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery

Post Operative Pain Clinical Trial

Official title:

A Single-dose, Open-Label, Multi-center Study to Assess the Safety and Preliminary Efficacy of PRF 110 (Formerly LNP) in Open Herniorrhaphy Surgery

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01681966
• Other study ID #: LNP-IL102
• Status: Completed
• Phase: Phase 2
• Start date: September 2012
• Est. completion date: May 4, 2016

Study information

• Verified date: November 2020
• Source: PainReform LTD
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

LNP is new extended release (ER) oily solution formulation of ropivacaine that is intended for local infiltration into surgical wounds. The purpose of this study is to determine the ease of usage and administration of LNP in the surgical setting, to follow the Pharmacokinetic (PK) profile of LNP over 72 hours and evaluate the duration of analgesia witnessed in the surgical setting.

Description:

LNP is new extended release (ER) oily solution formulation of ropivacaine that is intended for local infiltration into surgical wounds. The formulation is designed to slowly release the ropivacaine over 36-72 hours. By providing local analgesia over a long time span, the need for systemic analgesics is expected to be reduced and hospital stays may be shortened. The purpose of this study is to determine the ease of usage and administration of LNP in the surgical setting, to follow the PK profile of LNP over 72 hours and evaluate the duration of analgesia witnessed in the surgical setting.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 15
• Est. completion date: May 4, 2016
• Est. primary completion date: May 4, 2016
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male subjects between 18-70 years of age who are scheduled to undergo open one sided herniorrhaphy surgery;
• Subjects have a BMI of less than 30 kg/m2;
• Subjects are in good physical health (other than the need for the surgical procedure) as judged by physical and laboratory examinations and have a negative urine based screen for drugs of abuse;
• Subjects must agree to refrain from ingesting any analgesic medication for at least 2 days (or 5 half-lives of the analgesic drug) prior to surgery; refrain from alcohol and excessive caffeine intake on the day of surgery and during 72 hours after surgery;
• Subject must be capable of reading, comprehending, and signing the informed consent form;

Exclusion Criteria:

• Subjects with a history of melena or any significant hepatic, renal, endocrine, cardiac, neurological, psychiatric, gastrointestinal, pulmonary, hematologic, or metabolic disorders;
• Subjects with a history of any type of cancer within 5 years of surgery;
• Subjects with any history of alcohol or substance abuse;
• Subjects that have a history of uncontrolled hypertension;
• Subjects with a known hypersensitivity to any local anesthetic drug;
• Subjects with a hemoglobin concentration of less than 10.0 g/dL;
• Subjects with any clinically significant abnormal lab result (as judged by the Principal Investigator);
• Subjects with atrial fibrillation/flutter, an inserted pacemaker, or complete left bundle branch block (LBBB) on ECG; or myocardial infarction within 6 months prior to surgery;
• Subjects with a clinically significant abnormal ECG at screening;
• Subjects with any condition or history judged by the Investigator to place the subject at increased risk;
• Subjects judged by the Investigator to be unable or unwilling to comply with the requirements of the protocol;
• Subjects who have used an investigational drug within 30 days prior to entering the study;
• Subjects who have donated blood within 3 months prior to the start of the study;
• Subjects who are members of the study site staff directly involved with the study or a relative of the Sponsor or other personnel involved with the study;

Related Conditions & MeSH terms

• Pain, Postoperative
• Post Operative Pain

Intervention

Drug:
• PRF110- oily solution (Ropivacaine)
Post operative application of PRF110-oily solution (Ropivacaine)

Locations

Country	Name	City	State
Israel	Western Galil Medical Center	Nahariya
Israel	Assaf Harofeh Medical Center	Rishon LeZion
Israel	Sourasky Medical Center	Tel Aviv

Sponsors (1)

Lead Sponsor	Collaborator
PainReform LTD

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Use of rescue medication	Overall use of rescue medication post operation	72 hours
Other	Maximum plasma concentration (Cmax)	Samples will be collected at designated times up to 72hrs post drug application	72 hrs
Primary	Incidence of treatment emergent adverse events (safety and tolerability).	All adverse events (AE) reported by the subjects will be recorded throughout the trial period	72 hours
Secondary	Post-operative Pain intensity	Pain on a scale of 0-10 assessed at 0,1,2,4,8,12,24,36,48,60,72hrs post operation will be used to evaluate pain intensity	72 hours