RECOVER-AUTONOMIC: Platform Protocol, Appendix A (IVIG)

Description

This study is a platform protocol designed to be flexible so that it is suitable for a wide range of settings within health care systems and in community settings where it can be integrated into COVID-19 programs and subsequent treatment plans. This protocol is a prospective, multi-center, multi-arm, randomized, controlled platform trial evaluating various interventions for use in the treatment of autonomic dysfunction symptoms, including cardiovascular complications and postural orthostatic tachycardia syndrome (POTS), in Post-Acute Sequelae of SARS-CoV-2 infection (PASC) participants. The interventions tested will include non-pharmacologic care and pharmacologic therapies with study drugs.

Conditions

Long COVID, Long Coronavirus Disease 2019 (Covid19), Long Covid-19

Study Overview

Study Details

Study overview

This study is a platform protocol designed to be flexible so that it is suitable for a wide range of settings within health care systems and in community settings where it can be integrated into COVID-19 programs and subsequent treatment plans. This protocol is a prospective, multi-center, multi-arm, randomized, controlled platform trial evaluating various interventions for use in the treatment of autonomic dysfunction symptoms, including cardiovascular complications and postural orthostatic tachycardia syndrome (POTS), in Post-Acute Sequelae of SARS-CoV-2 infection (PASC) participants. The interventions tested will include non-pharmacologic care and pharmacologic therapies with study drugs.

RECOVER-AUTONOMIC (IVIG): Randomized Trial of the Effect of IVIG Versus Placebo on Long COVID Symptoms

RECOVER-AUTONOMIC: Platform Protocol, Appendix A (IVIG)

Condition
Long COVID
Intervention / Treatment

-

Contacts and Locations

Durham

All sites listed under NCT06305780, Durham, North Carolina, United States, 27710

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * See NCT06305780 for RECOVER-AUTO: Platform Protocol level inclusion criteria which applies to this appendix (or sub-study)
  • * See NCT06305780 for RECOVER-AUTO: Platform Protocol level exclusion criteria which applies to this appendix (or sub-study)

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Kanecia Obie Zimmerman,

Christopher Grainger, MD, STUDY_CHAIR, Duke Clinical Research Institute

Cyndya Shibao, MD, STUDY_CHAIR, Vanderbilt University Medical Center

Peter Novak, MD, STUDY_CHAIR, Harvard

Pam Taub, MD, STUDY_CHAIR, University of California, San Diego

Tae Chung, MD, STUDY_CHAIR, Johns Hopkins University

Study Record Dates

2026-03