Sildenafil in Emergency Treatment of Biliary Colic: A pilot randomized controlled trial

Abstract

Background: Sildenafil was reported to have a strong inhibitory effect on both gallbladder contraction and biliary pressure of the Sphincter of Oddi. We hypothesized that a single oral dose of sildenafil might counteract the smooth muscle spasm and decrease the intra-ductal and sphincteric pressures to relieve the pain of biliary colic and facilitate the release of impacted stones. Objectives: To assess the pain-relieving effect of 25 mg oral Sildenafil dose in comparison to an oral 20 mg ketorolac dose in adult patients presenting with acute biliary colic. Methods: Twenty consecutive eligible patients presenting with moderate to severe biliary colic were randomly assigned to receive one Sildenafil 25 mg tablet or two ketorolac 10 mg oral tablets. A four-point verbal rating scale (VRS) and 100 mm Visual pain analog scale (VPAS) of pain severity were measured before treatment then at 30 and 60 minutes after the dose intake. Results: Treatment success, defined as a reduction of VRS, 60 minutes after dose intake from moderate and severe to mild or none was similar (9/10) in both treatment groups. Significant reductions of VPAS at 30 and 60 minutes were noted in both groups. The reduction in VPAS after 60 minutes from dose intake was significantly greater in the Sildenafil group (83.16%) than in the ketorolac group (79.34%) (p=0.033). Conclusions: Single oral dose of sildenafil 25 mg might be safe and effective for the relief of biliary colic. Further studies are needed to confirm its value, particularly for patients who cannot tolerate or show inadequate response to NSAIDs or opiates.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

ACTRN12619001388101 (https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=378014&isReview=true)

Funding Statement

This study did not receive any funding

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study protocol had been approved by the "Green Clinic and Research Center" institutional review board registered by FDA under the number: (IRB00008268) according to the Declaration of Helsinki ethical principles for medical research. All subjects gave written informed consent before performing any treatment intervention.

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Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines and uploaded the relevant EQUATOR Network research reporting checklist(s) and other pertinent material as supplementary files, if applicable.

Yes

Data Availability

All data produced in the present study are available upon reasonable request to the author.

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