# PRO STRESS Trial: Proactive Low-Dose Norepinephrine to Reduce Intraoperative Fluid Administration in Patients at High-Risk for Postoperative Pulmonary Complications Undergoing Laparoscopic Abdominal Surgery

> **NCT07627360** · NA · NOT_YET_RECRUITING · sponsor: **Suez Canal University** · enrollment: 130 (estimated)

## Conditions studied

- Intraoperative Hypotension
- Postoperative Pulmonary Complications (PPCs)
- Fluid Over-load

## Interventions

- **DRUG:** Norepinephrine
- **OTHER:** Placebo

## Key facts

- **NCT ID:** NCT07627360
- **Lead sponsor:** Suez Canal University
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2026-07-15
- **Primary completion:** 2026-10
- **Final completion:** 2026-11
- **Target enrollment:** 130 (ESTIMATED)
- **Last updated:** 2026-07-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07627360

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07627360, "PRO STRESS Trial: Proactive Low-Dose Norepinephrine to Reduce Intraoperative Fluid Administration in Patients at High-Risk for Postoperative Pulmonary Complications Undergoing Laparoscopic Abdominal Surgery". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07627360. Licensed CC0.

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