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NCT04631393: PACSPI-1

Patient-controlled Sedation in Port Implantation (PACSPI-1)

Completed Last updated 19 October 2021
What this trial tests

trial testing Propofol Alfentanil in Pain in 40 participants. Completed in 15 October 2021.

Timeline
14 April 2021
Primary endpoint
15 October 2021
15 October 2021

Quick facts

Lead sponsorStefanie Seifert
StatusCompleted
Study typeOBSERVATIONAL
Enrollment40
Start date14 April 2021
Primary completion15 October 2021
Estimated completion15 October 2021
Sites1 location across Sweden

Drugs / interventions tested

Conditions studied

Sponsor

Stefanie Seifert

Who can join

Adults 18 to 105, any sex, with Pain or Patient Satisfaction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this prospective, observational study is to assess the feasibility of patient-controlled sedation (PCS) for implantation of subcutaneous venous ports (SVP).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. Patient-Controlled Sedation in Port Implantation (PACSPI 1) - A feasibility trial.
    Seifert S, Taxbro K, Hammarskjöld F. · · 2022 · cited 2× · PMID 37588584 · DOI 10.1016/j.bjao.2022.100026
  2. Patient-Controlled Sedation in Port Implantation (PACSPI 1) – a Feasibility Trial
    Seifert S, Taxbro K, Hammarskjöld F. · · 2022 · DOI 10.21203/rs.3.rs-1305841/v1

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04631393.

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