Precise Endoscopic Application of Nitroglycerin in Preventing Post-ERCP Pancreatitis

ConditionPancreatitis
Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Cheng-Kung University Hospital

About this trial

Endoscopic retrograde cholangiopancreatography (ERCP) is a technically demanding procedure combining endoscopy and fluoroscopy to diagnose and treat pancreaticobiliary disorders such as bile duct stones, strictures, and cholangitis. Despite its therapeutic value, ERCP carries a relatively high complication risk of about 10%, with severe complications occurring in roughly 24% of those affected and mortality rates between 0.2% and 0.7%. The most common and significant complication is post-ERCP pancreatitis (PEP), occurring in 2% to 10% of average patients and up to 40% or higher in high-risk groups. PEP ranges from mild, self-limiting inflammation to severe, life-threatening conditions including pancreatic necrosis and multi-organ failure.

PEP arises from mechanical trauma, hydrostatic injury, chemical irritation, or infection during ERCP that activates inflammatory pathways within the pancreas. Key patient-related risk factors include young age, female sex, prior pancreatitis, and sphincter of Oddi dysfunction; procedural factors include difficult biliary cannulation, pancreatic duct manipulation, and precut sphincterotomy.

Preventive strategies focus on minimizing mechanical injury and pharmacologic prophylaxis. Rectal NSAIDs (indomethacin, diclofenac) administered immediately before ERCP are well-supported for reducing PEP risk. Periprocedural aggressive intravenous hydration and prophylactic pancreatic duct stenting in high-risk cases also lower PEP incidence.

Nitroglycerin, a smooth muscle relaxant acting via nitric oxide-mediated sphincter relaxation, has shown promise in PEP prevention, especially in patients contraindicated for NSAIDs. Clinical trials indicate that transdermal or sublingual nitroglycerin reduces PEP rates, and combined use with NSAIDs may enhance protection. However, current guidelines do not routinely recommend nitroglycerin due to limited consensus on its efficacy.

Topical nitroglycerin, known to relax smooth muscles locally and used in anorectal conditions, might reduce sphincter of Oddi pressure without systemic side effects. This suggests potential benefit in lowering PEP incidence or severity when applied topically during ERCP, pending further investigation. This study aimed to investigate whether topical delivery of nitroglycerin can reduce the incidence rate of PEP or the severity of pancreatitis.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Eligible participants include patients aged ≥ 18 years who accept ERCP and sphincterotomy for common bile duct (CBD) stone extraction.

Disqualifiers

patients with pancreatic cancer

shock status (systolic blood pressure < 90 mmHg or using inotropic agents)

allergy to NTG

angle-closure glaucoma

Trial design

Design model

Parallel

Treatments tested in this trial

  • Nitroglycerin (NTG)

    Drug

    All patients without chronic kidney disease (serum creatine \> 1.5 mg/dL) will receive rectal diclofenac 100 mg before the procedure. During the biliary cannulation, if twice or more times of pancreatic duct cannulation, a pancreatic plastic stent will be placed. Lactate ringer hydration will be provided to patients with pancreatic duct cannulation for 24 hours. After the EST and stone extraction, we will randomly assign the patients to either a control or an intervention group. After EST, if immediate bleeding occurs, we will apply standard endoscopic therapy by either local injection of diluted epinephrine or heater probe coagulation. Before the end of the exam, diluted 1mg nitroglycerin in normal saline (1mg/10cc) will be delivered to the major papilla in the intervention group, and 10cc normal saline will be delivered to the major papilla in the standard group.

  • Normal Saline (0.9% NaCl)

    Drug

    All patients without chronic kidney disease (serum creatine \> 1.5 mg/dL) will receive rectal diclofenac 100 mg before the procedure. During the biliary cannulation, if twice or more times of pancreatic duct cannulation, a pancreatic plastic stent will be placed. Lactate ringer hydration will be provided to patients with pancreatic duct cannulation for 24 hours. After the EST and stone extraction, we will randomly assign the patients to either a control or an intervention group. After EST, if immediate bleeding occurs, we will apply standard endoscopic therapy by either local injection of diluted epinephrine or heater probe coagulation. Before the end of the exam, diluted 1mg nitroglycerin in normal saline (1mg/10cc) will be delivered to the major papilla in the intervention group.

Treatment groups

440 Participants
are divided into 2 treatment groups
Group A: Intervention GroupExperimental treatment 1 intervention
Group B: Standard GroupPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Occurrence of Post-ERCP pancreatitis

Incidence of Post-ERCP pancreatitis based on a widely recognised Cotton consensus, which is defined as a three-fold increase of serum lipase at ≥24 h and necessitating hospital admission or prolonged hospital stay.

Time frame
7 days

Secondary outcomes

1

Occurence of moderate or severe PEP

The severity classification of PEP was also defined according to the Cotton criteria. The categories included: (1) mild: an extension of hospitalisation period of 2-3 days; (2) moderate: an extension of hospitalisation period of 4-10 days; (3) severe: an extension of at least 10 days, or haemorrhagic pancreatitis, phlegmon or pseudocyst, intervention (percutaneous drainage or surgery) or death.

Time frame
7 days
2

Occurrence of post-ERCP bleeding

All patients were monitored for 14 days after EST, either during hospitalization or outpatient follow-up. For patients reporting hematemesis or presenting with tarry or bloody stool, diagnostic endoscopy was performed to identify the source of bleeding.

Time frame
14 days
3

Occurrence of shock status

Hypotension with SBP \< 90mmHg or in need of inotropic agents after the application of NTG.

Time frame
1 day
4

Length of hospitalization

Length of hospitalization

Time frame
14 days

Other outcomes

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