Skip to content

Serum Parameter Prior and After EUS-guided Fine Needle Aspiration of the Pancreas

Serum Lipase, Amylase and CA 19-9 Prior and After EUS-guided Fine Needle Aspiration of the Pancreas

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02397993
Enrollment
208
Registered
2015-03-25
Start date
2015-03-31
Completion date
2020-12-31
Last updated
2019-02-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatitis

Brief summary

Endoscopic ultrasonography (EUS ) -guided fine needle aspiration (EUS -FNA ) of focal pancreatic lesions is an essential diagnostic procedure with high therapeutic effect in clinical routine. The aim of this study is to determine the levels of serum lipase, serum amylase and the tumor marker CA 19-9 prior and after EUS-FNA. In animal experiments on dogs, an increase of all three parameters was observed after surgery on the pancreas. For humans, these clinically important data are not yet available . It is assumed that the probability of pancreatitis with increased activity of lipase and amylase will rise with the number of puncture procedures as well as the size of the puncture needle. In addition, the post-interventional assessment of the tumor marker CA 19-9 could result in a false positive assumption of malignant neoplastic pancreatic lesion.

Interventions

PROCEDUREblood collection

blood will be taken for assessment of serum lipase, serum amylase and CA 19-9 prior to EUS-FNA

During endoscopic ultrasonography, fine needle aspiration will be performed for cytological analysis of the pancreas

Sponsors

Helios Albert-Schweitzer-Klinik Northeim
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* independent indication for pancreatic EUS-FNA * age ≥ 18 years * patient able to give informed consent

Exclusion criteria

* Contraindications for EUS-FNA * pregnancy * no informed consent available * known stenosis of esophagus or duodenum * relevant coagulation disorders

Design outcomes

Primary

MeasureTime frame
Serum lipaseup to 24h prior to EUS-FNA and 4 hours after EUS-FNA

Secondary

MeasureTime frame
CA 19-9up to 24 hours prior to EUS-FNA
Serum amylaseup to 24 hours prior to EUS-FNA

Countries

Germany

Contacts

Primary ContactTobias Meister, PD Dr.
tobias.meister@helios-kliniken.de+495551971244

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026