Urology Clinic, Harbor-UCLA Medical Center
Torrance, California, 90502, United States
NCT Number: NCT01756651
The purpose of this study is to assess the safety and efficacy of intranasally-administrated fentanyl pectin spray (Lazanda®)given to decrease the pain during cystoscopy (the passage of a telescopic instrument into the bladder for purpose of diagnosing the cause of blood in the urine, urinary complaints or any other problems with the urinary bladder). The current standard practice is to use Lidocaine jelly (a local anesthetic) given through the urethra to lubricate and decrease local pain. In this study, an additional medicine (Lazanda®) is used to reduce pain that occurs during and after the above procedure.
Looking for future studies?
Notify Me18 year and older
Male
Interventional
Phase 1
Torrance, California, 90502, United States
In this prospective study, twenty subjects will be enrolled. The first ten will receive a dose of 100mcg pectin fentanyl nasal spray (Lazanda®). The second ten will receive a dose of 200mcg pectin fentanyl nasal spray (Lazanda®) if the 100mcg was well tolerated in the first ten. In all cases, Lidocaine jelly is used as an local anesthetic in the urethra.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
comparison of Intranasal fentanyl 100mcg vs 200 mcg.
Other names: Lazanda, Fentanyl
Time frame: within 3 hours post administration of the drug
The primary endpoint is the worst pain experienced at any time during the procedure.
Pain will be assessed using the Numeric Rating Scale (NRS score 0 = no pain to 10 = worst possible pain).
Time frame: Every 5 minutes post administration of the drug until 3 hours
Pulse oximetry will be recorded at baseline and every 5 minutes for 3 hours post drug-administration.
Time frame: every 15 minutes until 3 hours post drug-administration
Will be recorded at baseline and every 15 minutes for 3 hours post drug-administration.
Richard C Reznichek, MD
Other
A Prospective Study Comparing the Efficacy and Safety of 100 mcg and 200 mcg of Intranasal Fentanyl Pectin Spray as an Analgesic in Adult Males Undergoing Outpatient Cystoscopic Procedures
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT01471639
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes
Cleveland, Ohio, United States
View Trial DetailsNCT01538745
Abdomen, Acute, Abdominal Pain
San Antonio, Texas, United States
View Trial DetailsNCT00802997
Chronic Pain, Neurologic Manifestations
Bradenton, Florida, United States
View Trial Details