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NCT07285863·Phase 4·INTERVENTIONAL

A Study Of Effect Of Secretin For In Injection (Chirostim) On Pancreatic Fluid Composition In Healthy Subjects

Status

Recruiting

Phase

Phase 4

Enrollment

24

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

The purpose of this study is to collect pancreas fluid from the duodenum using the endoscopic pancreas function collection method in healthy participants after pancreatic stimulation with human secretin.

Interventions

Treatment arms and agents.

DRUG

Secretin (human synthetic) - ChiRhoClin

During endoscopic ultrasound (EUS), a dose of intravenous secretin (0.2 µg/kg) will be administered over the course of 1 minute to stimulate pancreatic ductal cells to secrete pancreas fluid. Duodenal fluid will be aspirated through the echoendoscope in 5 minute increments (5, 10, 15, and 20 minutes) after the secretin has been administered

Timeline

From registration to results.

  1. First posted

    Dec 16, 2025

  2. Study start

    Mar 11, 2026

  3. Primary completion

    Mar 2027

  4. Study completion

    Mar 2028

  5. Results posted

    Not reported

  6. Registry updated

    Jul 7, 2026

Outcomes

What the study measures.

Primary outcomes

Pancreatic Fluid Bicarbonate Composition

Time frame · 5, 10, 15, and 20-minutes post-secretin administration

A primary outcome will be the bicarbonate level (milliequivalent per liter) in the pancreatic fluid collected.

Pancreatic Fluid Sodium Composition

Time frame · 5, 10, 15, and 20-minutes post-secretin administration

A primary outcome will be the sodium level (milliequivalent per liter) in the pancreatic fluid collected.

Pancreatic Fluid Potassium Composition

Time frame · 5, 10, 15, and 20-minutes post-secretin administration

A primary outcome will be the potassium level (milliequivalent per liter) in the pancreatic fluid collected.

Pancreatic Fluid Chloride Composition

Time frame · 5, 10, 15, and 20-minutes post-secretin administration

A primary outcome will be the chloride level (milliequivalent per liter) in the pancreatic fluid collected.

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
80 Years
Sex
ALL
Healthy volunteers
Yes

Inclusion Criteria * Males or non-pregnant females * Age 18-80. * Participants must be in good health based on medical history (ASA Class 3 or below) * Participants must be willing and able to provide informed consent * Receiving an endoscopic ultrasound for a non-pancreatic indication Exclusion Criteria * History of any form of pancreatitis and/or other pancreatic diseases (e.g. pancreatic cysts, pancreatic masses). * History of inflammatory bowel disease * History of vagotomy. * History of surgically altered upper gastrointestinal anatomy (e.g. gastric bypass, Billroth I/II) * History of liver disease * Pregnant women or nursing mothers * Regular use of anticholinergics * \> 2 drinks of alcohol daily * Smokers (cigarette)

Study locations

1 registered sites.

United States. Showing up to 24 locations stored in the fast local snapshot.

Mayo Clinic in Rochester

Rochester, Minnesota, United States

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Secretin.

Related PeptideStat pages

Put the record in context.

Research pages describe evidence. Vendor pages, where available, describe independently tracked research-product listings and are not clinical recommendations.