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NCT06151444
Intensive Versus Standard Treatment for Hypotension on Maternal Hemodynamics in Preeclamptic Patients
NA trial testing Alpha-Agonist in Adverse Effect in 160 participants. Status unknown.
31 December 2024
Quick facts
| Lead sponsor | General Hospital of Ningxia Medical University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 160 |
| Start date | 1 July 2024 |
| Primary completion | 31 December 2024 |
| Estimated completion | 31 December 2024 |
Drugs / interventions tested
- Alpha-Agonist — full drug profile →
- α-adrenergic receptor agonist — full drug profile →
Conditions studied
- Adverse Effect — all drugs for Adverse Effect →
Sponsor
General Hospital of Ningxia Medical University
Who can join
Adults 18 to 45, female only, with Adverse Effect. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The objective of this study is to investigate the impact of varying maternal blood pressure maintenance targets on maternal hemodynamics in preeclamptic patients following cesarean section.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06151444
- Europe PMC full search
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- ESMO Meeting Library
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Related trials
Other trials of Alpha-Agonist
Trials testing the same drug.
- NCT06151470 — 90% Effective Dose of Phenylephrine Infusions Under Intensive and Standard Treatment in Preeclamptic Patients · NA · unknown
- NCT06151522 — 90% Effective Dose of Phenylephrine Infusions Under Intensive and Standard Treatment · NA · unknown
- NCT06151509 — 90% Effective Dose of Norepinephrine Infusions Under Intensive and Standard Treatment · NA · unknown
- NCT06151457 — 90% Effective Dose of Norepinephrine Infusions Under Intensive and Standard Treatment in Preeclamptic Patients · NA · unknown
- NCT06151496 — Intensive Versus Standard Treatment for Spinal Anesthesia-induced Hypotension on Maternal Hemodynamics · NA · unknown
Other recruiting trials for Adverse Effect
Currently open trials in the same condition.
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- NCT06570616 — Addressing Unintentional Leakage When Using Nasal CPAP - Study A · NA · recruiting
- NCT06467045 — Frequency of Adverse Events in Pediatric Patients Receiving Sedation for Magnetic Resonance Imaging · recruiting
Other General Hospital of Ningxia Medical University trials
Trials by the same sponsor.
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- NCT07366853 — Feasibility and Safety of Sciatic Nerve Paraneural Sheath Block Using a Mid-Femoral Lateral Approach · NA · not yet recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06151444 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by General Hospital of Ningxia Medical University
- Last refreshed: 30 November 2023
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/NCT06151444.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing