Post-craniotomy

2

Review clinical trials related to Post-craniotomy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Pre-emptive Scalp Infiltration With Low-dose Flurbiprofen and Ropivacaine for Postoperative Analgesia After Craniotomy

Post-craniotomy pain is common and often associated with poor outcomes. Flurbiprofen axetil (FA) is an injectable NSAID for postoperative analgesia, however, the impact of local FA, remains elusive on post-craniotomy pain. As FA is highly lipophilic by merging into emulsified lipid microspheres, it has a high affinity to the surgical incision and inflammatory tissues to achieve targeted drug therapy and prolonged duration of action. On base of the previous report that local NSAIDs achieved therapeutic tissue concentrations despite a plasma concentration of \<5% of that of systemic administration, a low-dose of FA might be considered a preferential option for local infiltration to avoid anti-platelet related side effects, such as intra-cerebral bleeding. In this study, the investigators attempt to evaluate the clinical effects of pre-emptive scalp infiltration with low-dose FA and ropivacaine for postoperative analgesia after craniotomy.

Participants needed: 216
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Beijing Tiantan HospitalUpdated: Nov 17, 2025Locations: 1
Eligibility criteria

Age 18-64 years; [+3]

Glasgow Coma Scale <15; [+4]

Status: Recruiting

Scores in Critically Ill Patients After Craniotomy

This study planned to review patients admitted to three ICU wards at Beijing Tiantan Hospital between 2017 and 2020. It focused on adult patients who had undergone craniotomy and stayed in the ICU for more than 24 hours. Researchers intended to collect patient information, surgery details, complications, and outcomes from medical records. They also planned to gather routine scoring data used at the hospital and double-check its accuracy. Patients would be divided into two groups based on whether they survived or not, and the ability of different scoring systems to predict outcomes would be analyzed. Additionally, the study aimed to group patients by the type of surgery and assess how well the scoring systems predicted outcomes for each group.

Participants needed: 1,600
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Beijing Tiantan HospitalUpdated: Feb 11, 2025Locations: 1
Eligibility criteria

Patients admitted to the ICU wards between 2017 and 2020 [+2]

Pregnant or lactating women [+1]