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The efficacy of calcium ion channel blocker combined proton pump inhibitors for the treatment of Nutcracker esophagus

The efficacy of calcium ion channel blocker combined proton pump inhibitors for the treatment of Nutcracker esophagus - CCB combined PPIs for the treatment of NE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072174
Enrollment
Unknown
Registered
2023-06-05
Start date
2016-12-16
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Nutcracker esophagus

Interventions

Diltiazem combined Lansoprozle—Placebo group:Diltiazem 30mg Qid combined Lansoprozle 30mg Qd
Placebo treatment
Placebo—Diltiazem combined Lansoprozle group:Placebo treatment
Diltiazem 30mg Qid combined Lansoprozle 30mg Qd

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were as follows: 1) age between 15-75 years, good functions of cardiopulmonary, liver and kidney, without severe diseases; 2) diagnosed to be NE. Diagnosis of NE was based on Gothenburg and defined as any of the swallows with a contractile pressure greater than 180 mm Hg(1mmHg=0.133kPa).

Exclusion criteria

Exclusion criteria: Exclusion criteria were as follows: 1) 24-hour pH monitoring did not indicate pathological acid reflux; 2) with coronary artery disease, severe arrthymia or other severe heart diseases; 3) cannot endure invasive examinations, such as EGD, esophageal manometry and 24h pH monitoring; 4) chronic alcoholism (male with 40g/day, female with 20g/day); 5) known other primary esophageal motility diseases, such as achalasia, ect. 6) known esophageal or gastric malignant diseases; 7) with gastric or duodenum active ulcer; 8) history of endoscopic or surgical treatment of esophagus or gastric; 9) pregnancy or nursing at the time of treatment;10) refuse to participate the study.

Design outcomes

Primary

MeasureTime frame
Esophageal contractile pressure;Esophageal acid exposure;

Secondary

MeasureTime frame
Clinical symptoms;

Countries

China

Contacts

Public Contactsuyu He

Suining Central Hospital

hesuyu2009@163.com+86 180 0825 8565

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026