Peripheral Chemoreflex/Arterial Baroreflex Interaction in Patients With Electrical Carotid Sinus Stimulation

NCT02587533 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2018-01-09

No results posted yet for this study

Summary

Peripheral chemoreceptors and baroreceptors are located in close proximity in the carotid artery wall at the level of the carotid bifurcation. Baroreceptor stimulation lowers sympathetic activity and blood pressure. In contrast, chemoreceptor stimulation raises sympathetic activity and blood pressure. Thus, beneficial effects of electrical carotid sinus stimulation on blood pressure could be diminished by chemoreceptor overactivity and/or concomitant chemoreceptor activation through the device. Therefore, our study will assess baroreflex/chemoreflex interactions in patients with resistant hypertension equipped with carotid sinus stimulators. The study will inform us of potential additional anti-hypertensive benefits of simultaneous chemoreceptor denervation during electrode placement. Furthermore, the results may provide information about suitable electrode design to spare co-activation of peripheral chemoreceptors. Taken together, the study will help develop strategies for improving responder rate and efficacy of carotid sinus stimulators in patients with resistant hypertension.

Conditions

  • Hypertension, Resistant to Conventional Therapy

Interventions

OTHER

Hyperoxia without dopamine

Nearly complete hemoglobin oxygen saturation.

OTHER

Hyperoxia with dopamine

Nearly complete hemoglobin oxygen saturation. Dopamine dose 3 µg/kg/min.

OTHER

Hypoxia without dopamine

Target hemoglobin oxygen saturation (SpO2) 80%.

OTHER

Hypoxia with dopamine

Target hemoglobin oxygen saturation (SpO2) 80%. Dopamine dose 3 µg/kg/min.

Sponsors & Collaborators

  • Charite University, Berlin, Germany

    collaborator OTHER
  • Vanderbilt University School of Medicine

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • University of Bristol

    collaborator OTHER
  • Hannover Medical School

    lead OTHER

Principal Investigators

  • Jens Tank, MD · Hannover Medical School

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2017-12-31
Completion
2017-12-31

Countries

  • Germany

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02587533 on ClinicalTrials.gov