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Sepsis Abdominal / Post Abdominal Surgery / Ringer's Lactate Crystalloid Solutions · Interventional Study
ClinicalTrials.gov · September 10, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a completed clinical trial registry entry documenting a planned comparison of Ringer's Lactate versus Sterofundin/Plasmalyte as maintenance fluids in septic patients post-abdominal surgery. No results are posted in this registry record; the source describes study design, planned enrollment, and primary and secondary outcome measures only.
Interventional, Randomized, Parallel, Single masking, Treatment purpose. Post Abdominal Surgery, Sepsis Abdominal; age from 18 Years; to 80 Years. Intervention: Steroundin Group. Compared with: Ringer's Lactate Group — Active Comparator. n = 82. 1 site: Pakistan.
This is a completed clinical trial registry entry documenting a planned comparison of Ringer's Lactate versus Sterofundin/Plasmalyte as maintenance fluids in septic patients post-abdominal surgery. No results are posted in this registry record; the source describes study design, planned enrollment, and primary and secondary outcome measures only.
No results are reported in this registry record; efficacy and safety data are not available.
The source did not state who this applies to in practice.
This is a completed registry record with no posted results; the study design and planned endpoints are documented but outcome data are not reported in this source.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07239713). This is a study registration, not published results. Lead sponsor: CMH Lahore Medical College and Institute of Dentistry. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 82 participants (ACTUAL). Conditions: Post Abdominal Surgery, Sepsis Abdominal. Interventions: OTHER: Ringer's Lactate Crystalloid Solutions; OTHER: Sterofundin (Bolus of crystalloids). Primary outcome measures: serum lactate , Samples will be collected at baseline (preoperatively or immediately postoperatively) and at predefined intervals during the postoperative period (e.g., 24 and 48 hours after surgery).. Brief summary: The goal of this clinical trial is to compare the clinical effects of using Ringer's Lactate and Sterofundin/ Plasmalyte as maintenance fluids in adult patients who have undergone abdominal surgery and are septic. The primary outcome will be the change in serum lactate levels. Secondary outcomes will include renal function parameters, qSOFA scores, and the incidence of postoperative complications within the first 72 hours following surgery.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.