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Completed

NCT Number: NCT01756651

Intranasal Fentanyl for Management of Pain Associated With Cystoscopic Procedures

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.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Urology Clinic, Harbor-UCLA Medical Center

Torrance, California, 90502, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male adult patients scheduled for cystoscopy; additional procedures (e.g. ureteral stent placement, stent exchange, bladder biopsy, retrograde pyelogram) may be included.

Exclusion criteria

  • History of analgesic abuse or opioid tolerance
  • Allergy to fentanyl or to any of the components of Lazanda®
  • Acute/chronic nasal problems such as rhinitis or sinusitis
  • Acute bronchial asthma / upper airway obstruction
  • Presence of bradycardia or history of seizures
  • Concomitant use of drugs that inhibit cytochrome P450 isoenzyme 3A4 (e.g., ritonavir, ketoconazole, itraconazole, troleandomycin, clarithromycin, nelfinavir, nefazodone, amprenavir, aprepitant, diltiazem, erythromycin, fluconazole, fosamprenavir, monoamine oxidase inhibitors and verapamil) or exposure to these drugs 30 days prior to placement on the study.
  • Concomitant use of vasoconstrictive nasal decongestants (e.g., oxymetazoline, phenylephrine, xylometazoline)
  • Numeric Rating Scale (NRS) pain score more than 0 at baseline
  • Any situation or condition which, in the investigator's opinion, puts the subject at significant risk, or could confound the study results.

Treatment and study plan

Fentanyl pectin

Drug

comparison of Intranasal fentanyl 100mcg vs 200 mcg.

Other names: Lazanda, Fentanyl

Primary outcomes

  1. Change from baseline in pain numeric rating scale

    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).

Secondary outcomes

  1. Oxyhemoglobin saturation

    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.

Other outcomes

  1. Mean arterial blood pressure

    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.

Sponsors and collaborators

Lead sponsor

Richard C Reznichek, MD

Other

Collaborators

  • Depomed

Registry information

Official study title

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

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Dec 27, 2012
Registry last updated
May 11, 2017

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.

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